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
- 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