FDA Device recall Z-0533-2024
Medline Leg bag, REF DYND12574
- FDA Device
- Class II
- ongoing
- Published 2023-12-20
On 2023-12-20 the FDA classified a Class II recall of Medline Leg bag, REF DYND12574 by Medline Industries Northfield, citing undeclared latex.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0533-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-19 |
| Published | 2023-12-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Medline Industries Northfield |
| Distribution | n/a |
Product
Medline Leg bag, REF DYND12574
Reason
Undeclared latex
Identifiers
| code_info | UDI/DI 40080196990338 (case), 10080196990337 (insert), Lot Numbers: 48623040001, 48623050001, 48623060001, 48623080001 |
|---|
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-0533-2024%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.