Home › TELEFLEX INCORPORATED › PILLING
PILLING
TELEFLEX INCORPORATED · Model IPN029193 · UDI-DI 14026704642011
FAT
Prescription
8
510(k) clearances
36
Adverse events
2
Recalls
9
Facilities
Description
HURST TUNGSTEN FILLED BOUGIE 36 FRENCH
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2010-05-11 | Stryker Endoscopy | The silicone sheath component of the product detaches from the catheter upon removal of the e-kit from the body. |
| 2009-08-20 | Stryker Endoscopy | The silicone sheath component of the product detaches from the catheter during removal of the e-kit from the body. |
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 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.