PlainRecalls
FDA Devices Moderate Class II Ongoing

28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028

Reported: December 8, 2021 Initiated: October 15, 2021 #Z-0313-2022

Product Description

28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028

Reason for Recall

XXX

Details

Recalling Firm
Howmedica Osteonics Corp.
Distribution
Puerto Rico
Location
Mahwah, NJ

Frequently Asked Questions

What product was recalled?
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-028. Recalled by Howmedica Osteonics Corp..
Why was this product recalled?
XXX
Which agency issued this recall?
This recall was issued by the FDA Devices on December 8, 2021. Severity: Moderate. Recall number: Z-0313-2022.