Campylobacter Blood Free Selective Medium — Class III medical device recall Z-0284-2019
Terminated recall by Acumedia Manufacturers, Inc., reported 2018-11-07, distributed in FL, TN. The product is labeled with an incorrect expiration date.
| Recall number | Z-0284-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acumedia Manufacturers, Inc., Lansing, MI, United States |
| Recall initiated | 2018-08-02 |
| Classified | 2018-10-26 |
| Reported by FDA | 2018-11-07 |
| Terminated | 2021-01-13 |
| Distributed | FL, TN |
| Countries outside the US | BR, CA |
| Quantity | 93 bottles |
| Reason classes | labeling |
| Lot numbers | 110685B |
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 for recall
The product is labeled with an incorrect expiration date.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0284-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.