Medline recalls specific convenience kits with temperature probes due to a distribution error. Affected kits include models DYNJ88569 and variants with certain lot numbers. No immediate action is required but check your kit for the listed model numbers and lot codes.
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 convenience kits that include temperature probes because of a distribution error in the production process. This could lead to improper use of the probes, but the recall does not specify a risk of injury or harm.
The temperature probes in these kits were distributed with an error in the production control process. This could result in improper use of the probes, but the recall does not indicate a risk of injury or harm.
Healthcare workers and others using Medline convenience kits with the listed model numbers and lot codes are most at risk. The recall affects specific production batches sold between 2024 and 2025.
Check your Medline Convenience Kit for model numbers DYNJ88569, DYNJ88569A, DYNJ88569B, or DYNJ88569C. Look for lot numbers listed in the recall: 25ABO124, 24KBT583, 24KBB032, 25DBF217, 25JBP861, or 26ABE456.
Look for model numbers DYNJ88569, DYNJ88569A, DYNJ88569B, or DYNJ88569C on the kit and associated lot numbers.
No, the recall does not require stopping use. Check your kit for the listed model numbers and lot codes to see if it is affected.
The recall does not specify a remedy, so no action is needed unless you have the listed model numbers and lot codes.
The recall states there is no risk of injury or harm, but improper use could occur due to the distribution error.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2697-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2697-2026 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.
