Reported Nov 27, 2024 · Ongoing
JuggerLoc/ToggleLoc 2.9mm Drill Guide, Model number 110027357
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?
JuggerLoc/ToggleLoc 2.9mm Drill GuideModel number 110027357
- Lot codes and dates
- UDI-DI 00880304857254 Lots
000244632600024463330002452241000245337800024673420002476076000247607700024760780002481506000248172400024865400002486541000249025600024931070002496066000249771500024977160002500871000250087200025040260002504027000250403100025040320002504033000250403400025040350002504036000250403700025045460002513868000251798200025179830002527929000252793100025280420002528043000252804400025280450002544040000259261400025926150002592616000259261700025926180002602484000260248700026024900002614121000261412200026141230002624306
- UDI-DI 00880304857254 Lots
- Amount recalled
- 691 (US); 2,045 (OUS)
Where it was sold
- Nationwide
Why it was recalled
Firm received complaints reporting that guides were warped when pulled out of packaging. This issue may result in extension of surgery to find another product, or may lead to adverse local tissue reaction leading to surgical intervention.
This product could cause temporary or reversible health problems — stop using it.
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