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Medium risk Medical DevicesClass II

Medline Convenience Kits Recall

Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITHOTOMY PACK, Model Number: DYNJ83185A; 3) LAP BASIN, Model Numbe

Updated January 7, 2026

Medline is recalling Lithotomy Packs and Lap Basin kits because sterilization equipment calibration problems may have compromised the sterility of these medical devices. If not properly sterilized, these devices could pose an infection risk during medical procedures.

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: 1) Lithotomy Pack, Model Number DYNJ83185; 2) Lithotomy Pack, Model Number DYNJ83185A; 3) Lap Basin, Model Number DYNJVB91109D.

Am I affected

You're affected if you have any of these Medline Convenience Kits with model numbers DYNJ83185, DYNJ83185A (Lithotomy Packs), or DYNJVB91109D (Lap Basin) on hand. Check the model number on your package or purchase records.

What to do right now

Stop using these devices and contact Medline Industries, LP or your medical device supplier immediately to return the affected kits. Do not use them in medical procedures until you receive guidance from Medline.

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-2100-2026
Classification
Class II
Recalled
January 7, 2026
Read the official notice

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