Reported Jul 15, 2026 · Ongoing

Medline Convenience Kits

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

Medline Convenience Kits

4 of 4 products

Products covered by this recall
Model / numberProduct as published
DYNJ88569OPEN HEART PEDS PACK
DYNJ88569AOPEN HEART PEDS PACK
DYNJ88569BOPEN HEART PEDS PACK
DYNJ88569COPEN HEART PEDS PACK
Lot codes and dates

7 of 7 products

Products covered by this recall
#BarcodesProduct as published
11019845918233440198459182335Lot Number: 25ABO124; 2) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case)
21019845918233440198459182335Lot Number: 24KBT583; 3) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case)
31019845930964940198459309640Lot Number: 24KBB032; 4) DYNJ88569A, UDI-DI: 10198459309649(each), 40198459309640(case)
41019845950566940198459505660Lot Number: 25DBF217; 5) DYNJ88569B, UDI-DI: 10198459505669(each), 40198459505660(case)
51019845958587640198459585877Lot Number: 25JBP861; 6) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case)
61019845958587640198459585877Lot Number: 26ABE456; 7) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case)
7Lot Number: 25KBI025
Amount recalled
396 kits

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:39 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.