--- title: "Angiodynamics, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Angiodynamics, Inc. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/angiodynamics-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Angiodynamics, Inc. recall records **59** reported ongoing 59 records in this archive. Latest source date Mar 3, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog No.: 10707103; Product/UPN No.: H787107071035 (Box), H787107071030 (Pouch); Box Q...](https://isitonrecall.com/recall/fda-device-z-1856-2026-soft-vu-angiographic-catheter-pigtail-non-braided-soft-vu-pt-4f-x-100cm-035-nb-10sh-catalog-no-10707/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 100CM 035 NB 10SH; Catalog N...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1856-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UPN No.: H787107100135 (Box), H787107100130 (Pouch); Box Qua...](https://isitonrecall.com/recall/fda-device-z-1857-2026-soft-vu-angiographic-catheter-kumpe-non-braided-soft-vu-kmp-4f-x-40cm-038-nb-0sh-catalog-no-10710013/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1857-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog No.: 10714001; Product/UPN No.: H787107140015 (Box), H787107140010 (Pouch); Box ...](https://isitonrecall.com/recall/fda-device-z-1858-2026-soft-vu-angiographic-catheter-omni-flush-non-braided-soft-vu-of-4f-x-65cm-038-nb-6sh-catalog-no-1071/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 038 NB 6SH; Catalog ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1858-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.: 10714002; Product/UPN No.: H787107140025 (Box), H787107140020 (Pouch); Box Qu...](https://isitonrecall.com/recall/fda-device-z-1859-2026-soft-vu-angiographic-catheter-pigtail-non-braided-soft-vu-pt-4f-x-65cm-038-nb-10sh-catalog-no-107140/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1859-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog No.: 10714009; Product/UPN No.: H787107140095 (Box), H787107140090 (Pouch); Box...](https://isitonrecall.com/recall/fda-device-z-1860-2026-soft-vu-angiographic-catheter-berenstein-non-braided-soft-vu-ber-4f-x-65cm-038-nb-0sh-catalog-no-107/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 65CM 038 NB 0SH; Catalog...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1860-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog No.: 10714011; Product/UPN No.: H787107140115 (Box), H787107140110 (Pouch); Box ...](https://isitonrecall.com/recall/fda-device-z-1861-2026-soft-vu-angiographic-catheter-cobra-2-non-braided-soft-vu-cb2-4f-x-65cm-038-nb-0sh-catalog-no-107140/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 65CM 038 NB 0SH; Catalog ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1861-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (Pouch); Box Quan...](https://isitonrecall.com/recall/fda-device-z-1862-2026-soft-vu-angiographic-catheter-kumpe-non-braided-soft-vu-kmp-4f-x-65cm-038-nb-0sh-catalog-no-10714014/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1862-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalog No.: 10714016; Product/UPN No.: H787107140165 (Box), H787107140160 (Pouch); Bo...](https://isitonrecall.com/recall/fda-device-z-1863-2026-soft-vu-angiographic-catheter-berenstein-non-braided-soft-vu-ber-4f-x-100cm-038-nb-0sh-catalog-no-10/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Berenstein, Non-Braided; SOFT-VU BER 4F X 100CM 038 NB 0SH; Catalo...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1863-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box...](https://isitonrecall.com/recall/fda-device-z-1864-2026-soft-vu-angiographic-catheter-cobra-1-non-braided-soft-vu-cb1-4f-x-100cm-038-nb-0sh-catalog-no-10714/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1864-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog No.: 10714018; Product/UPN No.: H787107140185 (Box), H787107140180 (Pouch); Box...](https://isitonrecall.com/recall/fda-device-z-1865-2026-soft-vu-angiographic-catheter-cobra-2-non-braided-soft-vu-cb2-4f-x-100cm-038-nb-0sh-catalog-no-10714/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Cobra (2), Non-Braided; SOFT-VU CB2 4F X 100CM 038 NB 0SH; Catalog...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1865-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No.: 10714021; Product/UPN No.: H787107140215 (Box), H787107140210 (Pouch); Box Qua...](https://isitonrecall.com/recall/fda-device-z-1866-2026-soft-vu-angiographic-catheter-kumpe-non-braided-soft-vu-kmp-4f-x-100cm-038-nb-0sh-catalog-no-1071402/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 100CM 038 NB 0SH; Catalog No....](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1866-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB 0SH; Catalog No.: 10714024; Product/UPN No.: H787107140245 (Box), H787107140240 ...](https://isitonrecall.com/recall/fda-device-z-1867-2026-soft-vu-angiographic-catheter-sos-omni-selective-1-non-braided-soft-vu-so1-4f-x-80cm-038-nb-0sh-cata/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Sos Omni Selective (1), Non-Braided; SOFT-VU SO1 4F X 80CM 038 NB ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1867-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Catalog No.: 10714040; Product/UPN No.: H787107140405 (Box), H787107140400 (Pouch)...](https://isitonrecall.com/recall/fda-device-z-1868-2026-soft-vu-angiographic-catheter-headhunter-1-non-braided-soft-vu-hh1-4f-x-100cm-038-nb-0sh-catalog-no/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Headhunter (1), Non-Braided; SOFT-VU HH1 4F X 100CM 038 NB 0SH; Ca...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1868-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; Catalog No.: 10731401; Product/UPN No.: H787107314015 (Box), H787107314010 (Pouch...](https://isitonrecall.com/recall/fda-device-z-1869-2026-soft-vu-angiographic-catheter-straight-art-non-braided-soft-vu-str-art-4f-x-65cm-035-nb-0sh-catalog/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Straight Art, Non-Braided; SOFT-VU STR ART 4F X 65CM 035 NB 0SH; C...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1869-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog No.: 10732301; Product/UPN No.: H787107323015 (Box), H787107323010 (Pouch); Box ...](https://isitonrecall.com/recall/fda-device-z-1870-2026-soft-vu-angiographic-catheter-omni-flush-non-braided-soft-vu-of-4f-x-65cm-035-nb-6sh-catalog-no-1073/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided; SOFT-VU OF 4F X 65CM 035 NB 6SH; Catalog ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1870-2026%22) Mar 3, 2026 FDA device enforcement ### [Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quan...](https://isitonrecall.com/recall/fda-device-z-1871-2026-soft-vu-angiographic-catheter-kumpe-non-braided-soft-vu-kmp-4f-x-40cm-035-nb-0sh-catalog-no-10734301/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.:...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1871-2026%22) Mar 3, 2026 FDA device enforcement ### [AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 2 R/O 2CM; Catalog No.: 13709005; Product/UPN No.: H787137090055 (Box)...](https://isitonrecall.com/recall/fda-device-z-1872-2026-accuvu-angiographic-catheter-omni-flush-non-braided-with-2-r-o-markers-accu-vu-of-4f-x-70cm-035-nb-6/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 2 R/O Markers; ACCU-VU OF 4F X 70CM 0...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1872-2026%22) Mar 3, 2026 FDA device enforcement ### [AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F X 100CM 035 NB 6SH 10 R/O 6@1CM 4@5CM; Catalog No.: 13709604; Product/UPN No.: ...](https://isitonrecall.com/recall/fda-device-z-1873-2026-accuvu-angiographic-catheter-straight-flush-non-braided-with-10-r-o-markers-accu-vu-str-fl-4f-x-100c/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for AccuVu Angiographic Catheter, Straight Flush, Non-Braided, With 10 R/O Markers; ACCU-VU STR FL 4F...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1873-2026%22) Mar 3, 2026 FDA device enforcement ### [AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM 035 NB 6SH 21 R/O 1CM; Catalog No.: 13709704; Product/UPN No.: H787137097045 (Bo...](https://isitonrecall.com/recall/fda-device-z-1874-2026-accuvu-angiographic-catheter-omni-flush-non-braided-with-21-r-o-markers-accu-vu-of-4f-x-70cm-035-nb/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for AccuVu Angiographic Catheter, Omni Flush, Non-Braided, With 21 R/O Markers; ACCU-VU OF 4F X 70CM ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1874-2026%22) Mar 3, 2026 FDA device enforcement ### [AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035 NB 10SH 21 R/O 1CM; Catalog No.: 13709804; Product/UPN No.: H787137098045 (Box)...](https://isitonrecall.com/recall/fda-device-z-1875-2026-accuvu-angiographic-catheter-pigtail-non-braided-with-21-r-o-markers-accu-vu-pt-4f-x-70cm-035-nb-10s/) The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Austria, Australia, Belgium, Canada, China, Chile, Curacao, Czech Republic, Germany, Ireland, Israel, Italy, Lebanon,... [Official source for AccuVu Angiographic Catheter, Pigtail, Non-Braided, With 21 R/O Markers; ACCU-VU PT 4F X 70CM 035...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1875-2026%22) ## Reasons in these listed records - The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub. These examples come from this result page and are not a ranking of every recall reason. ## Checking Angiodynamics, Inc. ### Is there a recall on angiodynamics, inc. right now? This archive contains 59 records, including 59 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Angiodynamics, Inc.](https://isitonrecall.com/check/?q=Angiodynamics%2C%20Inc.) 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