Z-0786-2023 Class II Ongoing

Recalled by Biomerieux Inc — Hazelwood, MO

FDA device recall Z-0786-2023 was initiated by Biomerieux Inc on November 9, 2022 and is designated Class II. Reason for recall: As the temperature and time out of range was exceeded, product performances cannot be guaranteed The recall status is ongoing. Affected quantity: 1 unit.

Recall Details

Product Type
Devices
Report Date
January 11, 2023
Initiation Date
November 9, 2022
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 unit

Product Description

API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500

Reason for Recall

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

Distribution Pattern

US Nationwide distribution.

Code Information

UDI/DI 03573026048259, Batch Number 1009395530