Reported Aug 27, 2014 · Terminated
Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer
Zimmer, Inc.
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: Zimmer, Inc. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer
- Lot codes and dates
Item Number 00-1146-040045050055060065070075080085090095100-32
- Amount recalled
- 47,682 units total
This recall covers 16 products
The agency filed one notice per product. You are reading one of them; the other 15 are below.
3 more are in the archive.
Where it was sold
Why it was recalled
Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
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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