Every recall we track for Medical Action Industries, Inc. 306 — 22 in all — plus the complaints and injury reports the public filed about them.
Recall of Medical Action Industries Dialysis Change Tray Clear Sequence model 78791 due to improper silicone seal that may cause doming or tearing. Affected units sold with specific lot codes.
Medical Action Industries recalls Pack Angiography NCMC 3/Cs BANNER kits with Medline Namic Angiographic Star Off Handle Manifolds due to potential particulate in fluid paths that could enter blood circulation.
Recall of 5-unit medical catheter kits with potential syringe disconnection risk. Affected units have specific lot numbers and reference codes.
Medical Action Industries recalls foam protective pouches with incorrect GMDN codes due to mislabeled UDI. Affected models include 6010, 6010-1, 6060, and others. No immediate action required as the hazard is a labeling error.
Recalled Medical Action Industries IV Start Kits (100 kits/case) with saline syringes from specific lot numbers. These kits were recalled by the supplier due to potential safety issues.
Medical Action Industries recalls cardiac catheter introduction kits with REF 58647D. Affected units have specific lot numbers and UDI/DI codes. Consumers should contact the manufacturer for details.
Recall of 20-pack disposable scissors with debris. Stop using if you have these sterile medical instruments.
Medical Action Industries recalls Port Access Kits with incorrect IV Start Kit labeling. This labeling error may cause confusion in medical use. Affected kits have specific lot numbers and expiration dates.
Recall of B. Braun CARESITE Port Access Kit w/Tegaderm with incorrect expiration date. Products labeled with extended expiration date of 02/21/2024 instead of 02/10/2024.
Recall of Central Line Dressing Kit 20/Cs with shorter expiry date than labeled. Affected units expire 03/31/2024. No immediate action needed but check expiration dates.
Recall of disposable mosquito hemostats due to potential flaking metal and brown spots. Affected units have batch 0000274502, expiring 07/24/2025. Stop using immediately.
Recalled Medical Action Industries General Purpose Instrument Tray (REF 61209) may have flaking metal or brown spots causing injury during medical procedures.
Recalled disposable curved hemostats from Medical Action Industries may have flaking metal or brown spots. Affected units include specific batch numbers with expiration dates through 2025.
Recall of Medical Action Industries Minor Procedure Tray (REF 61214) due to potential flaking metal and brown spots on hemostats. Affected units have specific batch numbers and expiration dates.
Medical Action Industries recalls novaplus hemostats with potential flaking metal or brown spots. Affected kits have batch numbers 0000275724 (exp 02/15/2022) and 0000277619 (exp 04/15/2022).
Recalled Medical Action Industries Blood Culture Kit (Part 80076) has potential package breach risk. Affected kits may have compromised BD ChloraPrep 3mL applicator. Stop using immediately if you own this kit.
Medical Action Industries recalls 306 Injection Review Kit (Part 74736) due to potential package breach in BD ChloraPrep applicator. Affected units sold through specific channels until 02/28/2022.
Medical Action Industries 306 recalls its Midline Insertion DA Kit (Part 77981B) due to potential package breach in BD ChloraPrep applicator. Affected kits have specific lot numbers and expiration dates. Consumers should contact the company for details.
Recalled Medical Action Industries Blood Culture kits (part 80315D) have potential package breaches in the BD ChloraPrep 3mL applicator. Affected kits expired by July 2021. Contact for replacement.
Recalled Medical Action Industries CentralLineDresChange Kit (Part 79420) has potential package integrity issues with BD ChloraPrep applicator. Consumers should check kit details and contact manufacturer for remedy.
Medical Action Industries recalls LVAD dressing change kit (part 79544B) due to potential breach in BD ChloraPrep 3mL applicator packaging. Affected units were sold with specific lot numbers and expiration dates.
Medical Action Industries recalls certain CVC Clear Sequence Change Kits due to saline solution pH potentially exceeding USP standards (4.5-7.0). Affected kits include specific models and lot numbers listed in the recall notice.
