28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Reported: December 8, 2021 Initiated: October 15, 2021 #Z-0314-2022
Product Description
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Reason for Recall
There is a potential for the outer white Tyvek lid to debond from the sealed package.
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 6260-9-122. Recalled by Howmedica Osteonics Corp..
Why was this product recalled? ▼
There is a potential for the outer white Tyvek lid to debond from the sealed package.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 8, 2021. Severity: Moderate. Recall number: Z-0314-2022.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11