Medical Action Industries 306 recalls
Medical Action Industries 306 appears in 26 official U.S. recall notices indexed by RecallRadar, most recently on 2026-10-14.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 26 |
|---|---|
| Published | 2020-01-15 to 2026-10-14 |
| By agency | FDA Device (26) |
| By classification | Class II (15), Class I (10), Class III (1) |
| By status | terminated (17), ongoing (9) |
| Distribution named in notices | AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NE, OH, PA, RI, SC, TX, US, VA, WA |
Recalls
- Generic Name: Kit, Urine, Clean Catch Trade Name: Kit: Urinary Clean Catch 20/cs Model/Catalog Number: 76769 Lot Number: 333606 UDI-DI: 208…
FDA Device · Class III · 2026-10-14 · Medical Action Industries 306
Reason: An internal data-entry error caused kit lot 333606 to be labeled with an expiration date of March 31, 2027, instead of February 28, 2027. - Blood Culture Collection Venipuncture Kit 20/Cs, REF: 77451
FDA Device · Class II · 2026-09-23 · Medical Action Industries 306
Reason: 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 lea… - Kit: Single Shot Epidural 20/Cs, REF: 59553
FDA Device · Class I · 2026-09-16 · Medical Action Industries 306
Reason: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules
FDA Device · Class I · 2026-09-16 · Medical Action Industries 306
Reason: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility. - Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
FDA Device · Class II · 2026-08-12 · Medical Action Industries 306
Reason: Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal. - Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
FDA Device · Class I · 2026-08-05 · Medical Action Industries 306
Reason: 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 b… - Medical Action Industries Inc
FDA Device · Class I · 2026-05-13 · Medical Action Industries 306
Reason: 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" - Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250 ea…
FDA Device · Class II · 2024-09-18 · Medical Action Industries 306
Reason: 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 misclassif… - IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile
FDA Device · Class II · 2024-04-03 · Medical Action Industries 306
Reason: The kits contain saline flush syringes which were recalled by the supplier. - Medical Action Industries Inc
FDA Device · Class II · 2022-12-28 · Medical Action Industries 306
Reason: Scissors contained debris. - Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
FDA Device · Class II · 2022-12-28 · Medical Action Industries 306
Reason: XXX - Medical Action Industries Inc
FDA Device · Class II · 2022-12-14 · Medical Action Industries 306
Reason: 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. - B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 11/23/2022)
FDA Device · Class II · 2022-11-30 · Medical Action Industries 306
Reason: The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024. - Kit: Central Line Dres Change 20/Cs
FDA Device · Class II · 2021-10-27 · Medical Action Industries 306
Reason: The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date. - Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
FDA Device · Class II · 2021-06-30 · Medical Action Industries 306
Reason: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits - Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
FDA Device · Class II · 2021-06-30 · Medical Action Industries 306
Reason: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits - Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
FDA Device · Class II · 2021-06-30 · Medical Action Industries 306
Reason: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits - Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
FDA Device · Class II · 2021-06-30 · Medical Action Industries 306
Reason: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits - novaplus, General Purpose Kit, Cat
FDA Device · Class II · 2021-06-30 · Medical Action Industries 306
Reason: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits - Kit: Midline Insertion DA. MAI Kit Part Number: 77981B
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Kit: LVAD Dres Chg
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Kit: Blood Culture
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Kit: Blood Culture MAI Kit Part Number: 80076
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Kit: Injection REVIEW MAI Kit Part Number: 74736
FDA Device · Class I · 2021-05-19 · Medical Action Industries 306
Reason: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator. - Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit, REF 77070B ***DIALYSI…
FDA Device · Class II · 2020-01-15 · Medical Action Industries 306
Reason: The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.