Palcam Agar Base — Class III medical device recall Z-0283-2019
Terminated recall by Acumedia Manufacturers, Inc., reported 2018-11-07, distributed nationwide. Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distribu
| Recall number | Z-0283-2019 |
|---|---|
| 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 | 2020-12-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, GB, MX, UY |
| Quantity | 22 bottles |
| Reason classes | labeling |
| Lot numbers | 110321B |
Product
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans.
Reason for recall
Expiration date on the label is incorrect. Correct expiration date was November 30, 2020 and label on distributed product listed the expiration date as November 30, 2021.
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-0283-2019. 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.