Remington MEDICAL Drainage Bag — Class II medical device recall Z-0487-2024
Ongoing recall by Remington Medical, Inc., reported 2023-12-13, distributed in FL, PA. There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
| Recall number | Z-0487-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remington Medical, Inc., Alpharetta, GA, United States |
| Recall initiated | 2023-11-03 |
| Classified | 2023-12-05 |
| Reported by FDA | 2023-12-13 |
| Distributed | FL, PA |
| Quantity | 3,080 devices |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20813079020008 |
| Lot numbers | 2325111 |
| Model numbers | 600-D |
Product
Remington MEDICAL Drainage Bag, REF 600-D;
Reason for recall
There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
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-0487-2024. 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.