FDA Device Intelligence
HomeTELEFLEX INCORPORATED › HUDSON RCI

HUDSON RCI

TELEFLEX INCORPORATED · Model IPN042682 · UDI-DI 34026704595038

FQZ Prescription
10
510(k) clearances
6
Adverse events
2
Recalls
46
Facilities

Description

Disposable Thermometer with Thermometer Adaptor

Recalls

DateFirmReason
2023-05-10BearCare, Inc.There have been reports of skin burns to children wearing the device.
2013-07-10Medical Indicators, Inc.TempaDot products may have been mislabeled.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.