PlainRecalls
FDA Devices Moderate Class II Ongoing

Medline Leg bag, REF DYND12578

Reported: December 20, 2023 Initiated: October 19, 2023 #Z-0534-2024

Product Description

Medline Leg bag, REF DYND12578

Reason for Recall

Undeclared latex

Details

Units Affected
19406 devices
Distribution
US and Panama
Location
Northfield, IL

Frequently Asked Questions

What product was recalled?
Medline Leg bag, REF DYND12578. Recalled by MEDLINE INDUSTRIES, LP - Northfield. Units affected: 19406 devices.
Why was this product recalled?
Undeclared latex
Which agency issued this recall?
This recall was issued by the FDA Devices on December 20, 2023. Severity: Moderate. Recall number: Z-0534-2024.