FDA Device recall Z-0487-2024
Remington MEDICAL Drainage Bag, REF 600-D
- FDA Device
- Class II
- ongoing
- Published 2023-12-13
On 2023-12-13 the FDA classified a Class II recall of Remington MEDICAL Drainage Bag, REF 600-D by Remington Medical, citing there is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0487-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-11-03 |
| Published | 2023-12-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Remington Medical |
| Distribution | FL, PA |
Product
Remington MEDICAL Drainage Bag, REF 600-D;
Reason
There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.
Identifiers
| code_info | UDI/DI 20813079020008, Lot Number 2325111 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0487-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.