Reported Nov 18, 2020 · Terminated
OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails
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 Intremedullary Knee Arthrodesis (IKA) nails
- Lot codes and dates
- Lot and Use by Date
296 of 296 codes
MS1709826R5/14/2025MS1202321R4/21/2025MS1506568R5/14/2025MS1506568R5/14/2025MS1202321R17/16/2025MS1709826R17/16/2025MS1710592R4/21/2025MS1506583R5/14/2025MS1609272R5/14/2025MS1710592R17/16/2025MS1405272R7/16/2025MS1609272R17/16/2025MS1506583R17/16/2025MS1609591R4/21/2025MS1609591R15/14/2025MS1609591R15/14/2025MS1709825R7/16/2025MS1609591R27/16/2025MS1710265R4/21/2025MS1609590R4/21/2025MS1711008R15/14/2025MS1609083R7/16/2025MS1711008R27/16/2025MS1710265R17/16/2025MS20142654/17/2025MS20142654/17/2025MS1710921R4/27/2025MS20142654/17/2025MS1710921R17/16/2025MS1912442R17/16/2025
- Lot and Use by Date
- Amount recalled
- 306 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.
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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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