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Medical Action Industries, Inc. 306 Recalls
22 recalls on record · January 15, 2020 to August 12, 2026 · Medical Devices
Recalls by year
20
21
22
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 12, 2026Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Hazard: Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
August 5, 2026Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
Hazard: 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.
May 13, 2026Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Hazard: 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"
September 18, 2024Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/
Hazard: 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.
April 3, 2024Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Hazard: The kits contain saline flush syringes which were recalled by the supplier.
December 28, 2022Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/
Hazard: Scissors contained debris.
December 28, 2022Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Hazard: XXX
December 14, 2022Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc
Hazard: 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.
November 30, 2022Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls B. Braun CARESITE Port Access Kit w/Tegaderm, REF 375214, Central Venous (cardiac) Catheter Tray (REF number corrected 1
Hazard: The kits were incorrectly labeled with an extended expiration date of 02/21/2024 instead of 02/10/2024.
October 27, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: Central Line Dres Change 20/Cs
Hazard: The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.
June 30, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC., Minor Procedure Tray, REF 61214
Hazard: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
June 30, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209
Hazard: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
June 30, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls novaplus, General Purpose Kit, Cat. No. 56603
Hazard: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
June 30, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC., Disposable Instrument Pack Curved Hemostat, REF 56224
Hazard: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
June 30, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC., Disposable Instrument Pack Mosquito Hemostat, REF 56220
Hazard: There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: Blood Culture MAI Kit Part Number: 80076
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: Blood Culture. MAI Kit Part Number: 80315D
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: LVAD Dres Chg. MAI Kit Part Number: 79544B
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: Midline Insertion DA. MAI Kit Part Number: 77981B
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: Injection REVIEW MAI Kit Part Number: 74736
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
May 19, 2021Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420
Hazard: Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
January 15, 2020Medical DevicesFDA
Medical Action Industries, Inc. 306 recalls Medical convenience trays and kits, labeled as: Medical Action Industries, Inc.: ***CVC*** Clear Sequence Change Kit
Hazard: The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.