FDA Device recall Z-1772-2026
MicroScan Neg MIC 3J REF C54814
- FDA Device
- Class II
- ongoing
- Published 2026-04-15
On 2026-04-15 the FDA classified a Class II recall of MicroScan Neg MIC 3J REF C54814 by Beckman Coulter, citing due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1772-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-25 |
| Published | 2026-04-15 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Beckman Coulter |
| Distribution | n/a |
Product
MicroScan Neg MIC 3J REF C54814
Reason
Due to a manufacturing issue - missing a drug in well 4/4 but contain double the amount of antibiotics
Identifiers
| code_info | Catalog Number: C54814 UDI code: N/A Lot Number: 2025-08-23 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1772-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.