Brand
Medical Action Industries, Inc. 306
2 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Medical Action Industries, Inc. 306 and translate it into plain English — free weekly digest, optional same-day alerts.
- 2024-09-18FDA-DeviceClass IIFoam 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 (40 each/case), 6805 (50 each/case), 6805-1 (175 each/case), 6810 (50 each/case), 6810-1 (350 each/case), 6830 (8 rolls/case), and 6860 (8 rolls/case)
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.
- 2024-04-03FDA-DeviceClass IIIV 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.
Get notified about new Medical Action Industries, Inc. 306 recalls
Free weekly digest. We email when a new federal recall affects Medical Action Industries, Inc. 306 or anything else in your household.
Get the Sunday Brief