Medline recalls two convenience kits with temperature probes that may have been distributed incorrectly. Affected kits include specific model numbers and lot numbers. Consumers should check their kits and contact Medline for details.
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.
Medline is recalling two types of convenience kits that contain temperature probes. The recall is due to a potential distribution error that could affect the probes' safety.
The recall is for a distribution error in the production of temperature probes. This error could lead to improper use or safety issues if the probes are not functioning correctly.
Users of Medline Convenience Kits with the specific model numbers DYNJ88569D and DYNJ901348F are affected. Healthcare workers and others using these kits for temperature monitoring are most at risk.
Check for model numbers DYNJ88569D (OPEN HEART PEDS PACK) or DYNJ901348F (ACCESSORY KIT). The lot numbers 26DBP363 and 25JBQ159 are also associated with these models.
Look for model numbers DYNJ88569D or DYNJ901348F on the kit packaging.
Reach out to Medline Industries for specific instructions on how to handle the recalled kits.
The recall is due to a distribution error that could affect the temperature probes' safety.
Model numbers DYNJ88569D (OPEN HEART PEDS PACK) and DYNJ901348F (ACCESSORY KIT) are affected.
Check for model numbers DYNJ88569D or DYNJ901348F and lot numbers 26DBP363 or 25JBQ159.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2696-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2696-2026 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
