Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement… — Class II medical device recall Z-2584-2017
Terminated recall by Acumedia Manufacturers, Inc., reported 2017-06-21, distributed nationwide. Contamination of product with possible Bacillus spp
| Recall number | Z-2584-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Acumedia Manufacturers, Inc., Lansing, MI, United States |
| Recall initiated | 2015-11-30 |
| Classified | 2017-06-14 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2017-11-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, EC, SG |
| Quantity | 28 units |
| Lot numbers | 108044 |
Product
Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is used with PALCAM Agar or PALCAM Broth as a supplement for the selective and differential enrichment of Listeria spp. From foods, dairy and environmental samples.
Reason for recall
Contamination of product with possible Bacillus spp
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-2584-2017. 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.