Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
C-Flow Bag Decanter Recalled by Microtek Medical Inc. Due to During sterile barrier testing performed on the decanter...
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 Microtek Medical Inc. directly.
Affected Products
C-Flow Bag Decanter, REF 2000S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
Quantity: 10,366 cases (518,300 units)
Why Was This Recalled?
During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Microtek Medical Inc.
Microtek Medical Inc. has 8 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report