Recall Z-0534-2024— MEDLINE INDUSTRIES, LP - Northfield
Class II · Ongoing
Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2023-10-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline Leg bag, REF DYND12578. Reason: Undeclared latex.
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-10-19
- Firm location
- Northfield, IL, United States
Product description
Medline Leg bag, REF DYND12578
Reason for recall
Undeclared latex
Data sourced from openFDA. This site is unofficial and independent of the FDA.