Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Foam Protective Pouches Recalled by Medical Action Industries, Inc. 306 Due to The protective pouches were identified to have been...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medical Action Industries, Inc. 306 directly.
Affected Products
Foam 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)
Quantity: 5,981,534 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medical Action Industries, Inc. 306
Medical Action Industries, Inc. 306 has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report