Recall Z-2072-2015— Biomet, Inc.
Class II · Terminated
Class II FDA medical device recall by Biomet, Inc., initiated 2015-06-17, terminated 2016-03-22. FDA's recall record names no specific 510(k) clearance for this event. Product: A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.. Reason: 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..
- Recalling firm
- Biomet, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2015-06-17
- Terminated
- 2016-03-22
- Firm location
- Warsaw, IN, United States
Product description
A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.