Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia) Recalled by Merete Medical GmbH Due to Mislabeling
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
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Quantity: 215 units
Why Was This Recalled?
Product may be mislabeled.
Where Was This Sold?
This product was distributed to 5 states: CA, IL, MD, NJ, OH
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