Class II — Remington Medical, Inc.
| Recalling firm | REMINGTON MEDICAL, INC. |
|---|---|
| Registered facility | View this company's 3 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | There is an error with the "Use by Date" and "Date of Manufacturer" on the box label. |
| Product | Remington MEDICAL Drainage Bag, REF 600-D; |
| Quantity | 3080 devices |
| Distribution | US: PA and FL |
| Initiated | 2023-11-03 |
| Classified | 2023-12-05 |
| Recall number | Z-0487-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Remington Medical, Inc. (Z-0487-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93377/
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