SM DIS Vol/dors RAD LAT COL Plate recall
SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204…
Why was SM DIS Vol/dors RAD LAT COL Plate 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
- SM DIS VOL/DORS RAD LAT COL PLATE, Item Nos. 47235801404 47235802102 47235802103 47235802104 47235802106 47235802108 47235802203 47235802204…
- 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)