FDAFDA · Food and drugs·Recall number Z-2119-2026
Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L
Published May 13, 2026 · Recall initiated: January 7, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Medline Industries, LP
- Distributor
- Worldwide - US Nationwide distribution.
- Lot
- 1) DYNJ50806L, UDI-DI: 10195327344672(each), 40195327344673(case), Lot Number: 23FBK937
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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