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.
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: 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.
See all 3 products in this recall →Related recalls
Same manufacturer · Medline Industries, LP
See all →- SevereMedline Bariatric Rollator Recalled Due to Front Wheel Assembly Disconnect Risk
FDA (Devices) · 2026-10-14
- SevereMedline Bariatric Rollator Recalled Due to Front Wheel Detachment Risk
FDA (Devices) · 2026-10-14
- SevereMedline Homecare Bed Hand Pendants Recalled for Fire Hazard
FDA (Devices) · 2026-10-07
- SevereMedline Homecare Beds Recalled for Fire Hazard in Hand Control Pendant
FDA (Devices) · 2026-10-07
- HighMedline Instrument Channel Brush Kits Recalled for Sharp Edges
FDA (Devices) · 2026-09-30
Same hazard · distribution control error
See all →- ModerateMedline Open Heart Peds Pack Convenience Kits Temperature Probe Recall
FDA (Devices) · 2026-07-15
- ModerateMedline Anesthesia Kit Peds Contains Defective Temperature Probes
FDA (Devices) · 2026-07-15
Similar recalls
- HighMedline Medical Convenience Kits Recalled Due to Potential Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighMedline Convenience Kits recalled due to sterilization calibration issues
FDA (Devices) · 2026-05-13
- HighMedline Recalls 263 Surgical Convenience Kits Due to Contamination
FDA (Devices) · 2026-09-02
- HighMedline Medical Procedure Kits Recalled for Potential Sterility Compromise
FDA (Devices) · 2024-10-30
- ModerateMedline Convenience Kits sterilization calibration issue recalled
FDA (Devices) · 2026-05-13
- HighMedline Recalls 663 Surgical Convenience Kits Due to Contamination
FDA (Devices) · 2026-09-02