Reported Nov 18, 2020 · Terminated
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
Merete Medical GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Merete Medical GmbH · Alt-Lankwitz 102 · Berlin · N/A
Is this the product you have?
- OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)
- Lot codes and dates
- Lot number Use By Date
94 of 94 codes
MS1913183R5/12/2025MS1811576R7/22/2025MS1913047R6/3/2025MS1811577R7/22/2025MS1913048R6/3/2025MS1811578R7/22/2025MS1913048R17/22/2025MS1913049R6/3/2025MS1913049R6/3/2025MS1811579R7/22/2025MS1913050R6/3/2025MS1913050R6/3/2025MS1811580R7/22/2025MS1913051R6/3/2025MS1811581R7/22/2025MS1912629R6/3/2025MS1811650R7/22/2025MS1912633R6/3/2025MS1912633R6/3/2025MS1811651R7/22/2025MS1913077R6/3/2025MS1913077R6/3/2025MS1811608R7/22/2025MS1913078R6/3/2025MS1811609R7/22/2025MS1913079R6/3/2025MS1811652R7/22/2025MS1913080R6/3/2025MS1811653R7/22/2025MS1912634R6/3/2025
- Lot number Use By Date
- Amount recalled
- 215 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Product may be mislabeled.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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