Peri Dist Volar/dorsal T/dorsal Delta Radial recall
PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 00234801308 00234801310 00234801312 00234801403…
Why was Peri Dist Volar/dorsal T/dorsal Delta Radial 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?
All product manufactured prior to January 2014.
- Product
- PERI DIST VOLAR/DORSAL T/DORSAL DELTA RADIAL, Item Nos. 00234801303 00234801304 00234801306 00234801308 00234801310 00234801312 00234801403…
- 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)