PlainRecalls
FDA Devices Moderate Class II Ongoing

32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032

Reported: February 23, 2022 Initiated: December 21, 2021 #Z-0644-2022

Product Description

32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032

Reason for Recall

There is a potential for the outer Tyvek lid to de-bond from the sealed package.

Details

Recalling Firm
Howmedica Osteonics Corp.
Units Affected
8 units
Distribution
Worldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.
Location
Mahwah, NJ

Frequently Asked Questions

What product was recalled?
32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032. Recalled by Howmedica Osteonics Corp.. Units affected: 8 units.
Why was this product recalled?
There is a potential for the outer Tyvek lid to de-bond from the sealed package.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 23, 2022. Severity: Moderate. Recall number: Z-0644-2022.