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…
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…
Read the official notice →- Date
- 2024-09-18
- Country
- United States
- Brand
- Medical Action Industries
- Product
- Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75 each/case), 6106 (250…
- Classification
- Class II
- Units
- Nationwide distribution. International distribution to Canada.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Medical Action Industries recalls
- 2026-08-12
USMedical Action Industries, Inc. 306 recalls Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of CA.Official notice →- 2026-08-05
- US
Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds
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…
- 2026-05-13
- US
Medical Action Industries, Inc. 306 recalls 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"
FDA · DeviceMedical Action Industries, Inc. 306US distribution to state of: AZ OUS: NoneOfficial notice → - 2024-04-03
- US
Medical Action Industries, Inc. 306 recalls 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.
FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the states of MN and ND. There as no…Official notice → - 2022-12-28
- US
Medical Action Industries, Inc. 306 recalls Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box,…
Scissors contained debris.
FDA · DeviceMedical Action Industries, Inc. 306Distribution was made to FL, IL, IN, MA, MD, MO, OH, and VA. There was no…Official notice → - US
Medical Action Industries, Inc. 306 recalls Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
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FDA · DeviceMedical Action Industries, Inc. 306US Nationwide distribution in the state of VA.Official notice →
Other drugs & medical recalls in the United States
- 2024-09-18
- US
Zimmer GmbH recalls Biolox Option Taper Sleeve, Type 1 Taper, -6mm Neck - Indicated for use in total hip replacement with cemented or non-cemented femoral and…
Mislabeled: Incorrect sleeve in the packaging. The outer packaging is labeled as a standard neck sleeve, however, the product within the box is a -6mm neck sleeve, and vice versa. The neck of the sleeve can be…
FDA · DeviceZimmer GmbHWorldwide distribution - US Nationwide and the countries of Japan, Netherlands.Official notice → - US
Technomed Europe recalls NEUROSIGN Disposable Stimulating Dissector, REF 5888-00
Product has have presence of brown discoloration or substance on the hinge area of the device
- US
Medtronic Xomed, Inc. recalls Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069
Product was distributed past expiration date.
FDA · DeviceMedtronic Xomed, Inc.International distribution to the country of Canada.Official notice → - US
Medtronic Perfusion Systems recalls Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
FDA · DeviceMedtronic Perfusion SystemsWorldwide distribution - US Nationwide and the countries of Cambodia, Greece,…Official notice → - US
Hitachi America, Ltd., Particle Therapy Division recalls Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A Software Version: N/A Product…
During positioning within the system's 3D to 3D matching mode while transferring CBCT images, when the Float Image Selection button is pressed, it may display CBCT images that are insufficient in number.
FDA · DeviceHitachi America, Ltd., Particle Therapy DivisionU.S. Nationwide distribution in the states of TN, TX, and WA.Official notice → - US
Fresenius Medical Care Holdings, Inc. recalls Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008…
Machines equipped with BPM3 Blood Pressure Modules (Blood pressure monitor TM-2917B with firmware version S005) will not record Blood Pressure measurements and does not alarm if the cuff tubing is kinked close to the…