G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended recall
G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to…
Why was G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended recalled?
The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.
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?
Item #110024464 Lot# 478340
- Product
- G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to…
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 8
- Distribution
- US Nationwide Distribution
- Recall date
- February 21, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)