Rescue M00538350Recalls & reported problems
Anrei Medical(HZ) Co.,Ltd. · Rescue Single Use Grasping Forceps · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 16948318903983), received between Sep 24, 2020 and Sep 24, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Tear, Rip or Hole in Device Packaging” (1 report).
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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Tear, Rip or Hole in Device Packaging1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2020Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A RESCUE RETRIEVAL FORCEPS WAS TO BE USED IN A PROCEDURE ON (B)(6) 2020. ACCORDING TO THE COMPLAINANT, DURING PREPARATION, SCRATCHES WERE FOUND ON THE SIDE OF THE WHITE PRODUCT PACKAGING AND WAS TORN OUT. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10581109 ↗
Other Endoscopic Grasping/Cutting Instrument, Non-Powered devices
- diagnostic FTRD Set 13Ovesco Endoscopy AG · Endoscopic Grasping/Cutting Instrument, Non-Powered13 reports
- Single Use Retrieval Basket V FG-V422PROlympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered1 death11 reports
- Single Use Retrieval Basket V FG-V432POlympus Medical Systems Corp. · Endoscopic grasping/cutting instrument, non-powered11 reports
- n.a. 27074BKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- n.a. 27072AKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- Raptor 00711177US Endoscopy · Endoscopic grasping/cutting instrument, non-powered8 reports
- n.a. 27071TJKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered6 reports
- Raptor 00711178US Endoscopy · Endoscopic grasping/cutting instrument, non-powered5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page