Cable-ready Short GTR and Cable-ready Long GTR recall
CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202
Why was Cable-ready Short GTR and Cable-ready Long GTR recalled?
Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).
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?
77001932 77001933 77001878 62176030 62112090 62146839
- Product
- CABLE-READY SHORT GTR and CABLE-READY LONG GTR, Item Nos. 00223200201 00223200202
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 5,459,583 total devices
- Distribution
- Distributed nationwide.
- Recall date
- November 13, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)