Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire recall: Sterility Concern
Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2237-033-00 Product Usage: A single use surgical…
Why was Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire recalled?
Various Trauma Guide Wires- creases in the sealing area on the end opposite of the product's chevron opening compromising product sterility
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 lots expiring prior to September 30, 2023
- Product
- Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2237-033-00 Product Usage: A single use surgical…
- Recalling firm
- Zimmer Biomet, Inc.
- Quantity
- 2080
- Distribution
- Worldwide - US Nationwide Distribution Foreign: CANADA AUSTRALIA BRAZIL CHILE HONG KONG JAPAN MALAYSIA NETHERLANDS NICARAGUA SINGAPORE TAIWAN
- Recall date
- December 12, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)