FDA Enforcement Class II Ongoing

STRADIS HEALTHCARE, Vasc Vein, Item No.682-1583,

Recall: Z-0541-2023 · Reported December 21, 2022

Enforcement

Recall Number
Z-0541-2023
Event ID
91124
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Stradis Medical, LLC dba Stradis Healthcare
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
December 21, 2022
Initiation Date
November 2, 2022
Classification Date
December 14, 2022
Address
3025 Northwoods Pkwy, N/A, Peachtree Corners, GA, 30071-1524, United States

Description

STRADIS HEALTHCARE, Vasc Vein, Item No.682-1583,

Reason

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.

Code Info

UDI/DI (case) M75268215831, UDI/DI (kit)M75268215830, Serial/Lot Numbers: 22237491038

Distribution

US nationwide distribution, and Canada.

Quantity

20 units