FDA Enforcement Class II Ongoing

ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373

Recall: Z-0825-2023 · Reported January 11, 2023

Enforcement

Recall Number
Z-0825-2023
Event ID
91148
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Biomerieux Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
January 11, 2023
Initiation Date
November 9, 2022
Classification Date
January 4, 2023
Address
595 Anglum Rd, N/A, Hazelwood, MO, 63042-2320, United States

Description

ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373

Reason

As the temperature and time out of range was exceeded, product performances cannot be guaranteed

Code Info

UDI/DI 03573026377953, Batch Numbers: 1009371780

Distribution

US Nationwide distribution.

Quantity

2 units