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RUSCH

TELEFLEX INCORPORATED · Model IPN041863 · UDI-DI 04026704111671

BWC Prescription
1
510(k) clearances
22
Adverse events (2 deaths)
2
Recalls
15
Facilities

Description

EASYCRIC EMERGENCY CRICOTHYROTOMY SET, STERILE PACK

Recalls

DateFirmReason
2026-03-05Cook IncorporatedProducts from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2019-11-15Tytek Medical IncA defect involving an occluded needle was discovered during a training exercise.

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

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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.