--- title: "Medical Action Industries, Inc. 306 Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Medical Action Industries, Inc. 306 recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/medical-action-industries-inc-306/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Medical Action Industries, Inc. 306 recall records **8** reported ongoing 12 records in this archive. Latest source date Jul 23, 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 Jul 23, 2026 FDA device enforcement ### [Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules](https://isitonrecall.com/recall/fda-device-z-3106-2026-kit-epidural-pain-tqc-20-cs-ref-82465-containing-sodium-chloride-injection-0-9-usp-10ml-ampules/) Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. Class I Reported ongoing Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS. [Official source for Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml amp...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3106-2026%22) Jul 23, 2026 FDA device enforcement ### [Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules](https://isitonrecall.com/recall/fda-device-z-3107-2026-kit-single-shot-epidural-20-cs-ref-59553-kit-single-shot-epidural-20-cs-ref-83945b-containing-sodium/) Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. Class I Reported ongoing Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS. [Official source for Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Contai...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3107-2026%22) Jul 23, 2026 FDA device enforcement ### [Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B; Blood Culture Collection Kit, REF: 81834C. All containing BD ChloraPrep Clear ...](https://isitonrecall.com/recall/fda-device-z-3181-2026-blood-culture-collection-venipuncture-kit-20-cs-ref-77451-blood-culture-kit-20-cs-ref-81834b-blood-c/) Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue inf... Class II Reported ongoing Distribution: US Nationwide distribution in the states of OH, IN, NC. [Official source for Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451; Blood Culture Kit 20/Cs, REF: 81834B...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3181-2026%22) May 21, 2026 FDA device enforcement ### [Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791](https://isitonrecall.com/recall/fda-device-z-2858-2026-brand-name-medical-action-industries-product-name-dialysis-change-tray-clear-sequence-model-catalog/) Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal. Class II Reported ongoing Distribution: US Nationwide distribution in the state of CA. [Official source for Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Cat...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2858-2026%22) May 13, 2026 FDA device enforcement ### [Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds](https://isitonrecall.com/recall/fda-device-z-2792-2026-pack-angiography-ncmc-3-cs-banner-ref-ncag62i-containing-medline-namic-angiographic-star-off-handle/) Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels. Class I Reported ongoing Distribution: US: AZ, CO [Official source for Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off H...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2792-2026%22) Mar 17, 2026 FDA device enforcement ### [Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case](https://isitonrecall.com/recall/fda-device-z-2007-2026-medical-action-industries-inc-pack-cath-bhh-ref-bhca49k-sterile-eo-rx-only-qty-5-case/) Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold" Class I Reported ongoing Distribution: US distribution to state of: AZ OUS: None [Official source for Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2007-2026%22) Jun 11, 2024 FDA device enforcement ### [Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 each/case), 6141 (250 each/case), 6203 (...](https://isitonrecall.com/recall/fda-device-z-3129-2024-foam-protective-pouches-model-numbers-6010-50-each-case-6010-1-350-each-case-6060-8-rolls-case-6070/) The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN. Class II Reported ongoing Distribution: Nationwide distribution. International distribution to Canada. [Official source for Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 roll...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3129-2024%22) Jan 15, 2024 FDA device enforcement ### [IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.](https://isitonrecall.com/recall/fda-device-z-1394-2024-iv-start-kit-containing-1-saline-syringe-5ml-ref-74654-100-kits-case-sterile/) The kits contain saline flush syringes which were recalled by the supplier. Class II Reported ongoing Distribution: US Nationwide distribution in the states of MN and ND. There as no foreign/military/government distribution. [Official source for IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1394-2024%22) Nov 4, 2022 FDA device enforcement ### [Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit](https://isitonrecall.com/recall/fda-device-z-0751-2023-medical-action-industries-inc-port-a-cath-kit-ref-58647d-cardiac-catheter-introduction-kit/) XXX Class II Reported terminated Distribution: US Nationwide distribution in the state of VA. [Official source for Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0751-2023%22) Oct 12, 2022 FDA device enforcement ### [Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit co...](https://isitonrecall.com/recall/fda-device-z-0464-2023-medical-action-industries-inc-port-access-kit-ref-76511b-on-case-label-sterile-and-medical-action-in/) The Port Access Kits were incorrectly labeled as IV Start Kits on the kit label. The case label was correctly labeled as Port Access Kits. Class II Reported terminated Distribution: Distribution was made to MN. There was no foreign/government/military distribution. [Official source for Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0464-2023%22) Oct 12, 2022 FDA device enforcement ### [Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.](https://isitonrecall.com/recall/fda-device-z-0765-2023-medical-action-industries-inc-disposable-instrument-pack-littauer-scissor-ref-56247-packaged-1-packa/) Scissors contained debris. Class II Reported terminated Distribution: Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no foreign/government/military distribution. [Official source for Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0765-2023%22) Sep 15, 2022 FDA device enforcement ### [B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)](https://isitonrecall.com/recall/fda-device-z-0265-2023-b-braun-caresite-port-access-kit-w-tegaderm-ref-375214-central-venous-cardiac-catheter-tray-ref-numb/) The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024. Class II Reported terminated Distribution: US Nationwide distribution in the state of Pennsylvania. [Official source for B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0265-2023%22) ## Reasons in these listed records - Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Blood culture convenience kits contain a component subject to a drug recall that due to an an open or incomplete seal on the packaging of the applicator may compromise the component's sterile barrier and if used may lead to localized skin or soft tissue infection. - Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal. - Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within blood vessels. These examples come from this result page and are not a ranking of every recall reason. ## Checking Medical Action Industries, Inc. 306 ### Is there a recall on medical action industries, inc. 306 right now? This archive contains 12 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 Medical Action Industries, Inc. 306](https://isitonrecall.com/check/?q=Medical%20Action%20Industries%2C%20Inc.%20306) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)