Reported May 16, 2018 · Terminated
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended…
DePuy Mitek, Inc., a Johnson & Johnson Co.
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: DePuy Mitek, Inc., a Johnson & Johnson Co. · 325 Paramount Dr · Raynham, MA · 02767-5199
Is this the product you have?
- LATARJET EXPERIENCE
- Sharp Curved Ostetome Product UsageThe Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries
- Lot codes and dates
16D0116D0216K0117A0117B0117B02
- Amount recalled
- 84
Where it was sold
Why it was recalled
Reports of product loosening or coming unscrewed from the handle.
This product could cause temporary or reversible health problems — stop using it.
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