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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
| Date | Firm | Reason |
|---|---|---|
| 2017-06-14 | Medspira, Llc | Potential 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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Get your free API keyRead the docsData 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.
