Rescue M00527450Recalls & reported problems
Anrei Medical(HZ) Co.,Ltd. · Rescue Single Use Grasping Forceps · Class 2
Data updated Oct 16, 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 16948318903822), received between Apr 22, 2024 and Apr 22, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Packaging Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Packaging Problem1
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 22, 2024Unsealed Device Packaging; Packaging Problem; Unsealed Device Packaging; Packaging Problem
IT WAS REPORTED TO BOSTON SCIENTIFIC CORPORATION THAT A BOX OF THE RESCUE RETRIEVAL FORCEPS WAS RECEIVED AND UNPACKED ON AN UNKNOWN DATE. DURING UNPACKING, THE SEAL OF THE PRODUCT POUCH WAS PEELED OFF AND THE BOX WAS FLATTENED. THERE WAS NO PROCEDURE NOR PATIENT INVOLVED DURING THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19152597 ↗
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. 27072AKarl Storz GmbH & Co. KG · Endoscopic grasping/cutting instrument, non-powered9 reports
- n.a. 27074BKarl 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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