PlainRecalls
FDA Devices Moderate Class II Terminated

6.5MMX165MM CANNULATED SCREW

Reported: October 27, 2021 Initiated: September 20, 2021 #Z-0143-2022

Product Description

6.5MMX165MM CANNULATED SCREW

Reason for Recall

The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.

Details

Recalling Firm
Smith & Nephew, Inc.
Units Affected
5 units
Distribution
Worldwide distribution - US Nationwide distribution in the states of OK, TN and the country of Canada.
Location
Memphis, TN

Frequently Asked Questions

What product was recalled?
6.5MMX165MM CANNULATED SCREW. Recalled by Smith & Nephew, Inc.. Units affected: 5 units.
Why was this product recalled?
The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 27, 2021. Severity: Moderate. Recall number: Z-0143-2022.