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Medium risk Medical DevicesClass II

Medline Convenience Kits Recall

Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L

Updated January 7, 2026

Medline Convenience Kits (Model DYNJ50806L) have been recalled because sterilization equipment calibration problems may have compromised the sterility of these medical devices. Using a non-sterile device could increase infection risk.

Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on January 7, 2026. Details below.

What is recalled

Medline Convenience Kits, Model Number DYNJ50806L (WMC I D PACK-LF).

Am I affected

You're affected if you have Medline Convenience Kits with Model Number DYNJ50806L or labeled as WMC I D PACK-LF.

What to do right now

Stop using this product. Contact Medline Industries, LP directly for instructions on how to return the device or obtain a replacement.

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.

Brands affected

Medline Industries, LP
Source
FDA
Category
Medical Devices
Recall ID
fda-Z-2119-2026
Classification
Class II
Recalled
January 7, 2026
Read the official notice

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