FDA Device Intelligence
HomeDevice types › FFL

Dislodger, Stone, Basket, Ureteral, Metal

FDA product code FFL · Class 2 · Gastroenterology, Urology

377
Registered devices
6,077
Adverse events
10
Recalls
52
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2023-06-22Wilson-Cook Medical Inc.Non-conforming product may appear in the field as inability to advance or retract the basket, or the drive wire breaking or separating from handle (with or with
2023-06-22Wilson-Cook Medical Inc.Non-conforming product may appear in the field as inability to advance or retract the basket, or the drive wire breaking or separating from handle (with or with
2022-02-07Philips North America, LLCUpdate to instructions for use regarding the cleaning and disinfection process for the reusable probes.
2014-10-07C.R. Bard, Inc.The product is non-sterile.
2008-08-08Sterilmed IncSteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted becau
2005-12-20Boston Scientific CorpThe basket wire assembly may detach from the drive wire while in the patient.
2005-12-20Boston Scientific CorpThe basket wire assembly may detach from the drive wire while in the patient.
2004-10-27Cardinal HealthThe dispenser box was mislabeled with the wrong length and the wrong wire gauge.
2003-12-22C.R. Bard, Inc., Urological DivisionProduct packaging may contain holes compromising sterility.
2003-12-22C.R. Bard, Inc., Urological DivisionProduct packaging may contain holes compromising sterility.

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 docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.