Dislodger, Stone, Biliary

FDA product code LQR · Class 2 · Gastroenterology, Urology

137

Registered devices

847

Adverse events

Recalls

510(k) clearances

Devices with this code

Date	Firm	Reason
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2026-03-05	Cook Incorporated	Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
2009-01-08	Boston Scientific Corp	The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to b
2009-01-08	Boston Scientific Corp	The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to b
2009-01-08	Boston Scientific Corp	The ultraviolet light barrier on the pouch may be discolored, which will allow ultraviolet light into the package and may cause the latex retrieval balloon to b
2006-05-19	Boston Scientific Corp	Lack of assurance of sterility, as the sterile barrier may fail.
2006-05-19	Boston Scientific Corp	Lack of assurance of sterility, as the sterile barrier may fail.
2006-05-19	Boston Scientific Corp	Lack of assurance of sterility, as the sterile barrier may fail.
2006-05-19	Boston Scientific Corp	Lack of assurance of sterility, as the sterile barrier may fail.
2006-05-19	Boston Scientific Corp	Lack of assurance of sterility, as the sterile barrier may fail.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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