Unrated Medical device recall · FDA · Published May 28, 2026

Medline Convenience Kits: Temperature Probe Recall Due to Distribution Error

Medline recalls specific convenience kits containing temperature probes with a distribution error. Affected kits may have safety risks; contact Medline for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2695-2026Medical device Medline ›

Recall notice

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.

Take action

Contact the company

Recalling firmMedline Industries, LP3 Lakes Dr · Northfield, IL 60093-2753

✎ GovInfoNow plain-language explainer

Medline is recalling convenience kits that include temperature probes due to a distribution error. This could lead to safety risks if the probes are used improperly. Read more at govinfonow.com/recall/49059-medline-convenience-kits-temperature-probe-recall-due-to-distribution-error.

Source Summary by GovInfoNow · govinfonow.com/recall/49059-medline-convenience-kits-temperature-probe-recall-due-to-distribution-error · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2695-2026

Cite this page

“Medline Convenience Kits: Temperature Probe Recall Due to Distribution Error.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49059-medline-convenience-kits-temperature-probe-recall-due-to-distribution-error. Based on FDA recall #Z-2695-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2695-2026%22&limit=1).

The FDA announced on May 28, 2026, that Medline Industries, LP is recalling Medline Convenience Kits containing Covidien Mon-a-Therm temperature probes due to distribution errors. The agency issued recall number Z-2695-2026 for the voluntary Class II action.

How to tell if you have it

Brand: Medline
Product: ANESTHESIA KIT PEDS 90-LF
Model Number: DYNJAP10125A
Lot Number: 24JBR072
Units affected: 1400 kits

The hazard

The convenience kits contain Covidien Mon-a-Therm General Purpose Temperature Probes, Size 9 Fr. Medtronic issued a recall of specific production lots of these probes due to an error in its distribution control process.

Context

GovInfoNow's records show Medline Industries, LP has had 68 other recalls since July 31, 2025. Recent Medline actions include a Aug. 14, 2026, recall of Basic Homecare Beds for potential fire hazards and an Aug. 11, 2026, convenience kit recall for fungal contamination risk. Other recent recalls of similar products include the Covidien Mon-a-Therm Temperature Probe Recall (April 23, 2026), Omnicell i.v.Station Label Stock Recall (March 25, 2026), and ICU Medical Hotline Fluid Warming Set Recall (June 24, 2026).

How to tell if you have this one

Check for the model number DYNJAP10125A on the kit. The lot number 24JBR072 is also associated with the affected items.

Brand
Medline
Category
Medical device

FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.

Recall number	Product, codes & lots	Quantity
Z-2695-2026	Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A; 1) DYNJAP10125A, UDI-DI: 10198459112911(each), 40198459112912(case), Lot Number: 24JBR072	1400 kits
Z-2696-2026	Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F; 1) DYNJ88569D, UDI-DI: 10198459745775(each), 40198459745776(case), Lot Number: 26DBP363; 2) DYNJ901348F, UDI-DI: 10198459216213(each), 40198459216214(case), Lot Number: 25JBQ159	75 kits
Z-2697-2026	Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C; 1) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 25ABO124; 2) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 24KBT583; 3) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 24KBB032; 4) DYNJ88569A, UDI-DI: 10198459309649(each), 40198459309640(case), Lot Number: 25DBF217; 5) DYNJ88569B, UDI-DI: 10198459505669(each), 40198459505660(case), Lot Number: 25JBP861; 6) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case), Lot Number: 26ABE456; 7) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case), Lot Number: 25KBI025	396 kits

Based on the official FDA remedy

What to do — step by step

Check Kit Details
Look for the model number DYNJAP10125A and lot number 24JBR072 on the kit.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 48 days after the firm started it.

May 28, 2026Firm started the recall
Jul 8, 2026FDA classified it Class II
Jul 15, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/49059-medline-convenience-kits-temperature-probe-recall-due-to-distribution-error">Medline Convenience Kits: Temperature Probe Recall Due to Distribution Error (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2695-2026 (May 28, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2695-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.