Recall archive / FDA device enforcement
Medline Leg bag, REF URO12573 — FDA record Z-0535-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Oct 19, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medline Leg bag, REF URO12573
- Reason
- Undeclared latex
- Classification
- Class II
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 144 devices
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0535-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI/DI 20888277719290 (case), 10888277719293 (insert), Lot Numbers: 48623050001, 48623060001 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US and Panama
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Dec 20, 2023
- Recall initiation date
- Oct 19, 2023
- Center classification date
- Dec 12, 2023
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.