Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Merete PediatrOS RigidTack Recalled by Merete Medical GmbH Due to Incorrect marketing label (25 mm) was applied to...
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 Merete Medical GmbH directly.
Affected Products
Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only
Quantity: 26 units
Why Was This Recalled?
Incorrect marketing label (25 mm) was applied to product size 20 mm.
Where Was This Sold?
Domestic: Illinois; Foreign: Germany.
About Merete Medical GmbH
Merete Medical GmbH has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report