FDA Device recall Z-0143-2022
6.5MMX165MM CANNULATED SCREW
- FDA Device
- Class II
- terminated
- Published 2021-10-27
On 2021-10-27 the FDA classified a Class II recall of 6.5MMX165MM CANNULATED SCREW by Smith And Nephew, citing the product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0143-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-09-20 |
| Published | 2021-10-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Smith And Nephew |
| Distribution | US |
Product
6.5MMX165MM CANNULATED SCREW
Reason
The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
Identifiers
| code_info | Model 71106365S; Lot 20GT39417 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Smith And Nephew
- TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16, REF: 71760816
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FDA Device · Class II · 2025-12-24 · Smith And Nephew - META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
FDA Device · Class II · 2025-05-28 · Smith And Nephew - BIORAPTOR Suture Anchors
FDA Device · Class II · 2024-12-11 · Smith And Nephew - Tandem Intl Bipolar Cocr Shell/UHMWPE Liner, TI-6AL-4V Retaining Ring, 28MM I.D. 46 MM O.D., REF 71324046, sterile, femoral head bipolar co…
FDA Device · Class II · 2024-11-13 · Smith And Nephew
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0143-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.