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RUSCH

TELEFLEX INCORPORATED · Model IPN006960 · UDI-DI 24026704058413

GBT Prescription
3
510(k) clearances
14
Adverse events
1
Recalls
1
Facilities

Description

Rectal tube, 50 cm, open tip, 1 eye

Recalls

DateFirmReason
2017-06-14Medspira, LlcPotential failure in the balloon bond in the inner catheter stem, leading to the separation of the balloon from the inner stem, leaving it in the rectal cavity.

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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.