Atlas FDA

Medline Leg bag, REF DYND12574

FDA device recall Z-0533-2024 · posted 2024-09-30 · Open, Classified

Recall details

Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Reason for recall
Undeclared latex
Action taken
Medline issued a recall notice to its consignees on 10/16/2023 by USPS First Class Mail. The notice explained the issue, potential risk user, and requested destruction of the affected product at the consignee. Anyone who further distributed the product is directed to notify those to whom the product was distributed.
Root cause
Labeling mix-ups
Status
Open, Classified
Product code
FAQ
Quantity affected
28942 devices
Distribution
US and Panama
Date initiated
2023-10-19
Date posted
2024-09-30
Location
Northfield, IL

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