Medline Convenience Kits containing temperature probes recalled
Medline Industries is recalling Convenience Kits containing Covidien Mon-a-Therm General Purpose Temperature Probes due to an error in distribution control. The recall affects 75 kits distributed nationwide.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The FDA classified this as a Class II recall. The source text does not report any illnesses, injuries, or adverse events—only an error in distribution control. This is a precautionary recall without evidence of harm.
Plain-English summary
Medline Industries, LP is recalling Medline Convenience Kits that contain Covidien Mon-a-Therm General Purpose Temperature Probes (Size 9 Fr). The affected kits include the OPEN HEART PEDS PACK (Model Number: DYNJ88569D, Lot Number: 26DBP363) and ACCESSORY KIT (Model Number: DYNJ901348F, Lot Number: 25JBQ159). A total of 75 kits were distributed nationwide.
The recall was initiated due to an error in the distribution control process for the temperature probes. Medtronic, the manufacturer of the probes, identified the issue and issued the recall.
Consumers and healthcare facilities in possession of these kits should stop using the affected products. Contact Medline Industries, LP for instructions on return or replacement of the recalled kits.
The recalled product
- Product
- Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
- Manufacturer
- Medline Industries, LP
- Affected units
- 75
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (8)
- 1) DYNJ88569D
- UDI-DI: 10198459745775(each)
- 40198459745776(case)
- Lot Number: 26DBP363
- 2) DYNJ901348F
- UDI-DI: 10198459216213(each)
- 40198459216214(case)
- Lot Number: 25JBQ159
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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