Reported Nov 27, 2013 · Terminated
Juggerknotless Drill Bit, REF 110003173, Sterile, Single Use Product Usage: The Juggerknotless Soft Anchors are…
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: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Juggerknotless Drill Bit, REF 110003173, Sterile
- Single Use Product UsageThe Juggerknotless Soft Anchors are indicated for soft tissue reattachment procedures in the shoulder, foot/ankle, hand/wrist, and hip
- Lot codes and dates
- Catalog
110003173Lot 127480185420233500233520
- Catalog
- Amount recalled
- 25
Where it was sold
Why it was recalled
Investigation identified that the design of the drill bit may make the suture anchor difficult to insert into the bone. The implant may skip across the hole or miss the hole during insertion.
This product could cause temporary or reversible health problems — stop using it.
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