Raptor 00711177 (UDI 00816765011317)Recalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00816765011317), received between Aug 30, 2018 and Apr 17, 2024 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Break” (4 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 17, 2024Break; Break

  THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THE WIRE ON THE RAPTOR GRASPING DEVICE "BROKE" WHILE REMOVING A FOOD BOLUS. ANOTHER RAPTOR GRASPING DEVICE WAS SUCCESSFULLY UTILIZED, AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A DELAY. NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19129741 ↗
• MalfunctionDec 27, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  THE USER FACILITY REPORTED VIA MEDWATCH (B)(4), "WHILE ATTEMPTING TO REMOVE FOOD LODGED IN ESOPHAGUS WITH THE RAPTOR GRASPING DEVICE, THE WIRE CONNECTING THE GRASP BROKE. FOOD BOLUS WAS EVENTUALLY DISLODGED WITH ANOTHER PIECE OF EQUIPMENT." NO REPORT OF INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18400663 ↗
• MalfunctionJul 1, 2021Detachment of Device or Device Component

  THE DISTRIBUTOR REPORTED THAT DURING A PATIENT PROCEDURE UPON WITHDRAWAL OF THE RAPTOR GRASPING DEVICE, THE USER NOTED THAT PART OF JAW COMPONENT OF A RAPTOR GRASPING DEVICE HAD DETACHED. THE PROCEDURE WAS COMPLETED SUCCESSFULLY, NO REPORT OF HARM TO THE PATIENT.

  Patient problems: Insufficient Information

  MAUDE report 12103692 ↗
• MalfunctionJul 30, 2020Break; Difficult to Open or Close

  THE DISTRIBUTOR REPORTED THAT A RAPTOR GRASPING DEVICE WAS DAMAGED PRIOR TO USE AND COULD NOT BE CLOSED. THE DEVICE WAS NOT USED IN A PROCEDURE NOR INSERTED INTO THE ENDOSCOPE. THE PATIENT HAD NO CONTACT WITH THE DEVICE AND THERE WAS NO HARM TO THE PATIENT OR USER.

  Patient problems: No Patient Involvement

  MAUDE report 10346007 ↗
• MalfunctionMay 29, 2020Break

  THE DISTRIBUTOR REPORTED THAT THE CONTROL WIRE OF A RAPTOR GRASPING DEVICE BROKE DURING PROCEDURAL USE. THE JAWS OF THE DEVICE WERE LEFT IN AN OPEN POSITION AND IT COULD NOT BE WITHDRAWN THROUGH THE ENDOSCOPE, REQUIRING REMOVAL AND REPLACEMENT OF THE ENDOSCOPE TO COMPLETE THE PATIENT PROCEDURE. A PROCEDURAL DELAY WAS REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 10101283 ↗
• MalfunctionApr 4, 2019Break; Detachment of Device or Device Component

  REFERENCE USER FACILITY MEDWATCH REPORT #5084083. THE USER FACILITY REPORTED THAT A RAPTOR GRASPING DEVICE BROKE DURING A PROCEDURE, NECESSITATING RETRIEVAL OF A PORTION OR PORTIONS OF THE DEVICE. THERE WERE NO INJURIES ASSOCIATED WITH THE REPORTED EVENT.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8484171 ↗
• MalfunctionDec 19, 2018Detachment of Device or Device Component

  THE USER FACILITY REPORTED THE JAW COMPONENT OF A RAPTOR GRASPING DEVICE BECAME DETACHED DURING A PROCEDURE TO RETRIEVE A PLASTIC STENT. THE PROCEDURE WAS COMPLETED USING A SECOND RAPTOR DEVICE, WITH NO REPORT OF HARM TO THE PATIENT OR USER.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 8181566 ↗
• MalfunctionAug 30, 2018Mechanical Problem; Appropriate Device Problem Term/Code Not Available

  THE USER FACILITY REPORTED DURING A STENT POSITIONING PROCEDURE, THE RAPTOR GRASPING DEVICE FAILED TO RELEASE FROM THE STENT. THE USER FACILITY CUT THE HANDLE FROM THE RAPTOR DEVICE TO FREE THE STENT AND THE PROCEDURE WAS COMPLETED. THERE WAS NO REPORT OF HARM TO THE PATIENT OR USER.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7833903 ↗