FDA Device recall Z-2469-2017
VITEK¿ 2 Gram Positive Susceptibility card (AST-GP75), IVD, REF 415670, 20 cards per carton
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of VITEK¿ 2 Gram Positive Susceptibility card (AST-GP75), IVD, REF 415670, 20 cards per carton by Biomerieux, citing the integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2469-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-04-20 |
| Published | 2017-06-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Biomerieux |
| Distribution | US |
Product
VITEK¿ 2 Gram Positive Susceptibility card (AST-GP75), IVD, REF 415670, 20 cards per carton.
Reason
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Identifiers
| code_info | 2750173203 18/May/18 2750179103 24/May/18 2750210203 24/Jun/18 2750222103 06/Jul/18 2750236103 20/Jul/18 275023612…2750173203 18/May/18 2750179103 24/May/18 2750210203 24/Jun/18 2750222103 06/Jul/18 2750236103 20/Jul/18 2750236123 20/Jul/18 2750249103 02/Aug/18 2750277103 30/Aug/18 2750285103 07/Sep/18 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2469-2017%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.