Recall archive / FDA device enforcement
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DY... — FDA record Z-2697-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date May 28, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Medline Industries, LP
- Quantity
- 396 kits
- Agency-reported status
- Ongoing
- Source record identifier
- Z-2697-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 1) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 25ABO124; 2) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 24KBT583; 3) DYNJ88569, UDI-DI: 10198459182334(each), 40198459182335(case), Lot Number: 24KBB032; 4) DYNJ88569A, UDI-DI: 10198459309649(each), 40198459309640(case), Lot Number: 25DBF217; 5) DYNJ88569B, UDI-DI: 10198459505669(each), 40198459505660(case), Lot Number: 25JBP861; 6) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case), Lot Number: 26ABE456; 7) DYNJ88569C, UDI-DI: 10198459585876(each), 40198459585877(case), Lot Number: 25KBI025 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Nationwide distribution.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Jul 15, 2026
- Recall initiation date
- May 28, 2026
- Center classification date
- Jul 8, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.