FDA recall, , Moderate risk
Medline Convenience Kits
Medline Convenience Kits contain temperature probes with an error in their distribution control process.
Summary by Recall Canary from the FDA notice
What happened
Medline Industries, LP, of Northfield, Illinois, recalled Medline Convenience Kits because they contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr, and Medtronic recalled specific production lots of those probes due to an error in their distribution control process. The FDA added the recall to its Enforcement Report on July 8, 2026, and the company began the recall on May 28, 2026, with nationwide distribution in the US.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your kit affected?
3 products
Match your product and all the details in one listed combination.
A UDI-DI is the device identifier printed with the barcode on the device label.
Anesthesia Kit Peds 90-LF
- Model
- DYNJAP10125A
- UDI-DI
- 10198459112911
- Lot code
- 24JBR072
Open Heart Peds Pack
- Model
- DYNJ88569D
- UDI-DI
- 10198459745775
- Lot code
- 26DBP363
- Model
- DYNJ88569
- UDI-DI
- 10198459182334
- Lot code
- 25ABO124
- 24KBT583
- 24KBB032
- Model
- DYNJ88569A
- UDI-DI
- 10198459309649
- Lot code
- 25DBF217
- Model
- DYNJ88569B
- UDI-DI
- 10198459505669
- Lot code
- 25JBP861
- Model
- DYNJ88569C
- UDI-DI
- 10198459585876
- Lot code
- 26ABE456
- 25KBI025
Accessory Kit
- Model
- DYNJ901348F
- UDI-DI
- 10198459216213
- Lot code
- 25JBQ159
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Medline Industries, LPNorthfield, Illinois
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99196
- Recall numbers
- Z-2695-2026 to Z-2697-2026
All recalls from Medline Industries, LP
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
