Reported Nov 18, 2020 · Terminated
OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)
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 (humerus)
- Lot codes and dates
- Lot Number Use By Date
64 of 64 codes
MS1912994R6/4/2025MS1811555R7/24/2025MS1913023R6/4/2025MS1811556R7/24/2025MS1913024R6/4/2025MS1913024R6/4/2025MS1811557R7/24/2025MS1913027R6/4/2025MS1811585R7/23/2025MS1913028R6/4/2025MS1811604R7/23/2025MS1913029R6/4/2025MS1913029R6/4/2025MS1811605R7/23/2025MS1913038R6/4/2025MS1811606R7/23/2025MS1811607R6/4/2025MS1811607R17/23/2025MS1913039R6/4/2025MS1811624R7/23/2025MS1811673R6/4/2025MS1811625R7/23/2025MS1811673R17/23/2025MS1811634R6/4/2025MS1811634R17/23/2025MS1913041R6/4/2025MS1811623R7/24/2025MS1913042R6/4/2025MS1811635R7/24/2025MS1913043R6/4/2025
- Lot Number Use By Date
- Amount recalled
- 144 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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