Medline Convenience Kits: 1) Wmc I D Pack-lf, Model Number: Dynj50806l

Recall Summary Medline is recalling certain Convenience Kits (Model DYNJ50806L) because equipment used to sterilize and package them may not have been properly calibrated, which could affect whether the products are sterile. All affected kits were processed through sterilization, but the calibration problems mean their sterility cannot be guaranteed. This recall affects consumers who purchased this specific model kit.

Product

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

Reason

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.

Classification

Class I

Category

consumer product recall

Country

United States

Agency

FDA-DEVICES

Recall date

2026-01-07

Status

Open, Classified

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c98cee07-b1f3-46da-9d3b-5d7ae47441fa