FDA Device recall Z-0284-2019
Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter spp
- FDA Device
- Class III
- terminated
- Published 2018-11-07
On 2018-11-07 the FDA classified a Class III recall of Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter spp by Acumedia Manufacturers, citing the product is labeled with an incorrect expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0284-2019 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2018-08-02 |
| Published | 2018-11-07 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Acumedia Manufacturers |
| Distribution | FL, TN |
Product
Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter spp. In a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.
Reason
The product is labeled with an incorrect expiration date.
Identifiers
| code_info | lot #110685B |
|---|
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-0284-2019%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.