Z-2072-2015 Class II Terminated
FDA device recall Z-2072-2015 was initiated by Biomet, Inc. on Jun 17, 2015 and is designated Class II. 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. The recall status is terminated (terminated Mar 22, 2016). Affected quantity: 223.
Recall Details
- Product Type
- Devices
- Report Date
- Jul 22, 2015
- Initiation Date
- Jun 17, 2015
- Termination Date
- Mar 22, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 223
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.
Distribution Pattern
Domestic: TX NJ, NC, KY, MA, SD, MO, AL, IN, GA, AR International: Netherlands, Japan, Costa Rica
Code Information
Part Number: 816301006 Lot Numbers: 099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2072-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026