PlainRecalls
FDA Devices Moderate Class II Ongoing

HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,

Reported: December 21, 2022 Initiated: November 2, 2022 #Z-0557-2023

Product Description

HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,

Reason for Recall

Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.

Details

Units Affected
3 units
Distribution
US nationwide distribution, and Canada.
Location
Peachtree Corners, GA

Frequently Asked Questions

What product was recalled?
HENRY SCHEIN, Vas Reversal Pack, Item No.888-2549,. Recalled by Stradis Medical, LLC dba Stradis Healthcare. Units affected: 3 units.
Why was this product recalled?
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 21, 2022. Severity: Moderate. Recall number: Z-0557-2023.