Medline Leg bag — Class II medical device recall Z-0533-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2023-12-20. Undeclared latex
| Recall number | Z-0533-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2023-10-19 |
| Classified | 2023-12-12 |
| Reported by FDA | 2023-12-20 |
| Countries outside the US | PA |
| Quantity | 28,942 devices |
| Reason classes | undeclared allergen |
| UPC / GTIN / UDI-DI | 10080196990337, 40080196990338 |
| Lot numbers | 48623040001, 48623050001, 48623060001, 48623080001 |
| Model numbers | DYND12574 |
Product
Medline Leg bag, REF DYND12574
Reason for recall
Undeclared latex
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-0533-2024. 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.