Reported Jul 10, 2019 · Terminated
K-Wire Trochar Tip, Model Number 212000008 Product Usage: These DVR Express Disposable Instruments are used to…
Zimmer Biomet, 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 Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- K-Wire Trochar Tip
- Model Number 212000008 Product UsageThese DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma
- Lot codes and dates
- Lot Numbers
187764193497193567232280232683232684232685232686233858234049235477BFI0LJ8BFI0M5BBFI0MAVBFI0N16BFI0NNNI0N17I0N18BFI0LJ8RBFI0MAVRBF10LJ8BF10MAVBFIOLI8I0NNN
- Lot Numbers
- Amount recalled
- 3022 total
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
There is a potential for weak seals of the sterile packaging.
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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