FDA Device recall Z-0535-2024
Medline Leg bag, REF URO12573
- 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 URO12573 by Medline Industries Northfield, citing undeclared latex.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0535-2024 |
| 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 URO12573
Reason
Undeclared latex
Identifiers
| code_info | UDI/DI 20888277719290 (case), 10888277719293 (insert), Lot Numbers: 48623050001, 48623060001 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Other recalls by Medline Industries Northfield
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FDA Drug · Class II · 2025-09-03 · Medline Industries Northfield - Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH…
FDA Device · Class I · 2025-09-03 · Medline Industries Northfield
All Medline Industries Northfield recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0535-2024%22
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