Skip to content

Medline Industries, Inc. DYNJAP10125ARecalls & reported problems

Medline Industries, Inc. · ANESTHESIA KIT PEDS 90-LF · Class 1

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. May 28, 2026Class IIOpen, Classified

    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.

    Z-2695-2026 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Other Circuit, breathing (w connector, adaptor, y piece) devices

All Circuit, breathing (w connector, adaptor, y piece) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page