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Medline Anesthesia Kit Peds 90-LF
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MEDICAL DEVICE RECALLMODERATE

Medline Anesthesia Kit Peds 90-LF

Medline recalls Anesthesia Kit Peds 90-LF due to included temperature probe distribution error.

What to do

Check if your kit has model number DYNJAP10125A. Stop using the kit and contact Medline for instructions on returning the affected product and obtaining a replacement.

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

Why it was recalled

Medline is recalling its Anesthesia Kit Peds 90-LF convenience kit because it contains a Covidien Mon-a-Therm general purpose temperature probe (size 9 Fr) that was recalled by Medtronic due to an error in its distribution control process.

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.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification