A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual recall
A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
Why was A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part Number: 816301006 Lot Numbers: 099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524
- Product
- A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
- Recalling firm
- Biomet, Inc.
- Quantity
- 223
- Distribution
- Domestic: TX NJ, NC, KY, MA, SD, MO, AL, IN, GA, AR International: Netherlands, Japan, Costa Rica
- Recall date
- July 22, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)