Home › TELEFLEX INCORPORATED › UROLIFT
UROLIFT
TELEFLEX INCORPORATED · Model IPN923351 · UDI-DI 10814932020282
PEW
Prescription
1
510(k) clearances
471
Adverse events (12 deaths)
2
Recalls
9
Facilities
Description
UroLift 2 Implant Cartridge Handle Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-06-24 | Neotract Inc | There is the potential that during implant deployment, the device may not properly deliver a implant. |
| 2018-07-06 | Neotract Inc | Upon implant deployment, the Capsular Tab may not be delivered as the needle is retracted. In this failure mode, the needle is deployed into the prostate and retracted, leaving no |
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.