Aarau, N/A, Switzerland
Smith & Nephew Orthopaedics AG recalls
1 recall recorded since 2018, most recently on 22 July 2020. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 22 July 2020
- Terminated
- 21 August 2026
- Reason
- Multiple lots being recalled due to a product design issue
- Distribution
- Worldwide distribution - US Nationwide distribution including in the state of TN and the countries of AU, BE, CA, CH, ES, FR, GB, JP, NL, NO, PL, SG, ZA.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2827-2020
- POLARSTEM COLLAR Reamer Guide, Catalog Number: 75102205, UPC Codes: 00885556535493 - Product Usage: Once the appropriate trial rasp size is in place, the adapter is removed and the calcar reamer guide (75102205) is posit
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.