Reported Jul 10, 2019 · Terminated
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
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?
- DVR Crosslock ePAK Screw Driver
- Model Number 212000002 Product UsageThese DVR Express Disposable Instruments are used to facilitate implantation of orthopedic medical devices in trauma
- Lot codes and dates
- Lot NumbersBFIOLBJ I0N5P
235471235472235473235474235475187762193492193493193494193495193496193565BF10LBJBFI0LBJBFI0M9EBFI0N10BFI0N11BFI0P39I0N0XI0N0XRI0N0YI0N10I0N11I0N5BI0P39225207
- 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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