Skip to main content
Recall Canary
Medline Convenience Kits
← Back to all recalls
MEDICAL DEVICE RECALLMODERATE

Medline Convenience Kits

Medline recalls convenience kits with Medtronic temperature probes due to distribution error.

What to do

Check your kit's model number against the recalled list. If affected, stop using the temperature probe and contact Medline for instructions on returning the kit for a replacement or refund.

Posted
Updated
Recall No.
Z-2695-2026
Agency
FDA
Firm
Medline Industries, LP
Recall ID
99196
Status
ONGOING

Why it was recalled

Medline Industries is recalling certain convenience kits because they contain Covidien Mon-a-Therm general purpose temperature probes (size 9 Fr) that were recalled by Medtronic due to a distribution control error. The affected kits include the Open Heart Peds Pack (model DYNJ88569D), Accessory Kit (model DYNJ901348F), and Anesthesia Kit Peds 90-LF (model DYNJAP10125A).

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

ProductLot codeModelUDI-DI
ANESTHESIA KIT PEDS 90-LF24JBR072DYNJAP10125A10198459112911
OPEN HEART PEDS PACK26DBP363DYNJ88569D10198459745775
ACCESSORY KIT25JBQ159DYNJ901348F10198459216213
OPEN HEART PEDS PACK25ABO124, 24KBT583, 24KBB032DYNJ8856910198459182334
OPEN HEART PEDS PACK25DBF217DYNJ88569A10198459309649
OPEN HEART PEDS PACK25JBP861DYNJ88569B10198459505669
OPEN HEART PEDS PACK26ABE456, 25KBI025DYNJ88569C10198459585876

Where it was sold

Distributed nationwide.

Official source

View on U.S. Food and Drug Administration →

Other recent recalls from Medline Industries, LP

← Back to all recalls

Editorial summary by Recall Canary · last updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification