--- title: "Davol, Inc. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Davol, 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/davol-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Davol, Inc. recall records **8** reported ongoing 8 records in this archive. Latest source date Mar 25, 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 25, 2026 FDA device enforcement ### [Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.](https://isitonrecall.com/recall/fda-device-z-1896-2026-avitene-ultrafoam-microfibrillar-collagen-hemostat-8cm-x-6-25cm-x-1cm-catalog-number-1050030/) Potential for product to contain foreign matter, confirmed to be inspect fragments. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of China, South Korea. [Official source for Avitene Ultrafoam Microfibrillar Collagen Hemostat - 8cm x 6.25cm x 1cm. Catalog Number: 1050030.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1896-2026%22) Apr 25, 2023 FDA device enforcement ### [Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460](https://isitonrecall.com/recall/fda-device-z-2241-2023-ventralight-st-4-x-6-ellipse-with-echo-ps-catalog-number-5955460/) Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Belgium, Czech Republic, France, Germany, Ireland, Italy, Netherlands, Portugal, Slovakia, South Africa, Spain, Swede... [Official source for Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2241-2023%22) Apr 25, 2023 FDA device enforcement ### [Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction ...](https://isitonrecall.com/recall/fda-device-z-2242-2023-ventralight-st-4-5-circle-with-echo-ps-a-low-profile-bioresorbable-coated-permanent-mesh-with-a-pre/) Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Belgium, Czech Republic, France, Germany, Ireland, Italy, Netherlands, Portugal, Slovakia, South Africa, Spain, Swede... [Official source for Ventralight ST 4.5" Circle with Echo PS- A low profile, bioresorbable, coated, permanent mesh, wi...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2242-2023%22) Apr 25, 2023 FDA device enforcement ### [Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of s...](https://isitonrecall.com/recall/fda-device-z-2243-2023-ventralight-st-w-echo-ps-4-5-circle-a-low-profile-bioresorbable-coated-permanent-mesh-with-a-pre-att/) Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Belgium, Czech Republic, France, Germany, Ireland, Italy, Netherlands, Portugal, Slovakia, South Africa, Spain, Swede... [Official source for Ventralight ST w Echo PS 4.5" Circle A low profile, bioresorbable, coated, permanent mesh, with a...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2243-2023%22) Apr 25, 2023 FDA device enforcement ### [Ventralight ST w EchoPS 4"x6" Ellipse- A low profile, bioresorbable, coated, permanent mesh, with a pre-attached removable positioning system, designed for the reconstruction of...](https://isitonrecall.com/recall/fda-device-z-2244-2023-ventralight-st-w-echops-4-x6-ellipse-a-low-profile-bioresorbable-coated-permanent-mesh-with-a-pre-at/) Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Belgium, Czech Republic, France, Germany, Ireland, Italy, Netherlands, Portugal, Slovakia, South Africa, Spain, Swede... [Official source for Ventralight ST w EchoPS 4"x6" Ellipse- A low profile, bioresorbable, coated, permanent mesh, with...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2244-2023%22) Jun 27, 2022 FDA device enforcement ### [X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Catalog No. 9551000)](https://isitonrecall.com/recall/fda-device-z-1457-2022-x-stream-irrigation-system-catalog-no-5551000-and-x-stream-irrigation-system-refurbished-catalog-no/) The device may potentially cause a fire, leading to a safety risk. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Canada and Chile. [Official source for X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Cata...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1457-2022%22) Jun 7, 2022 FDA device enforcement ### [HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880](https://isitonrecall.com/recall/fda-device-z-1304-2022-hydrosurg-plus-laparoscopic-irrigator-with-nezhat-dorsey-smokevac-trumpet-valve-handle-only-with-coj/) The product is not able to provide irrigation. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, wit...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1304-2022%22) Jun 7, 2022 FDA device enforcement ### [HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Cojoined Suction and Irrigation Tubing, Catalog Number 0026870](https://isitonrecall.com/recall/fda-device-z-1305-2022-hydrosurg-plus-laparoscopic-irrigator-with-nezhat-dorsey-smokevac-trumpet-valve-33cm-tip-and-cojoine/) The product is not able to provide irrigation. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the country of Canada. [Official source for HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, 33cm Tip and Coj...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1305-2022%22) ## Reasons in these listed records - Potential for product to contain foreign matter, confirmed to be inspect fragments. - Balloon may not inflate as intended. If the balloon does not inflate during laparoscopic ventral hernia repair this may result in a delay or prolongation of the procedure, inadequate mesh placement, erosion/migration, pain and mesh infection - The device may potentially cause a fire, leading to a safety risk. - The product is not able to provide irrigation. These examples come from this result page and are not a ranking of every recall reason. ## Checking Davol, Inc. ### Is there a recall on davol, inc. right now? This archive contains 8 records, including 8 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 Davol, Inc.](https://isitonrecall.com/check/?q=Davol%2C%20Inc.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)