Reported Jul 22, 2015 · Terminated
A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
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?
- A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
- Lot codes and dates
- Part Number816301006
- Lot Numbers
099216093776093717093716088526081179072525072524
- Amount recalled
- 223
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
Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.
This product could cause temporary or reversible health problems — stop using it.
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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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