Medline Anesthesia Kit Peds Contains Defective Temperature Probes
Medline Industries is recalling Anesthesia Kit Peds (Model DYNJAP10125A, Lot 24JBR072) nationwide because they contain Covidien Mon-a-Therm temperature probes affected by a distribution control error.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: This is an FDA Class II recall of a medical device. The source text does not report any injuries, illnesses, or hospitalizations related to the distribution control error, and the hazard is preventable through kit identification and discontinuation of use.
Plain-English summary
Medline Industries, LP is recalling the Anesthesia Kit Peds 90-LF (Model Number DYNJAP10125A) distributed nationwide. The kits contain Covidien Mon-a-Therm General Purpose Temperature Probes, Size 9 Fr, which were subject to an error in the distribution control process.
Affected kits bear Lot Number 24JBR072. The recall affects approximately 1,400 kits. Healthcare facilities and providers who have received these kits should identify and discontinue use of affected units.
Patients and healthcare providers with questions about this recall should contact Medline Industries, LP or consult the FDA's recall notice at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=Z-2695-2026.
The recalled product
- Product
- Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
- Manufacturer
- Medline Industries, LP
- Affected units
- 1,400
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 (4)
- 1) DYNJAP10125A
- UDI-DI: 10198459112911(each)
- 40198459112912(case)
- Lot Number: 24JBR072
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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