Medline Industries, Lp: Circuit, Breathing (w Connector, Adaptor, Y Piece)
Recall Summary Medline Anesthesia Kits for pediatric patients (Model DYNJAP10125A) are being recalled nationwide because they contain temperature probes from Medtronic that were distributed in error due to a control process failure. The affected kits were distributed across all U.S. states and the District of Columbia. This is classified as a Class I recall, the most serious classification.
- Recalling firm
- Medline Industries, LP
- Product
- Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
- 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 I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-28
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e9cc69fa-20d5-4932-b6d4-57d0ebf38c38