Kevorkian-Pacific biopsy punch 64-675Recalls & reported problems
Coopersurgical, Inc. · Kevorkian-Pacific biopsy punch- length: 22 cm; bite: 9 mm x 3mm · Class 1
Data updated Oct 18, 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 00888937017489), received between Oct 6, 2020 and Oct 6, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Device” (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 18, 2026.
Most reported problems
Device problems
- Defective Device1
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.
MalfunctionOct 6, 2020Defective Device
CUSTOMER STATED: "DEFECTIVE - CANNOT OPEN TO UTILIZE. PROVIDER NEEDED TO DO A BIOPSY AND THE FORCEP DID NOT OPEN, IT WAS JAMMED. - PATIENT WAS NOT INJURED DURING THE PROCEDURE". 1216677-2020-00225-1 64-675 KEVORKIAN-PACIFIC PUNCH E-COMPLAINT (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10637032 ↗
Other Forceps, Biopsy, Gynecological devices
- Trinity Sterile, Inc. 96-4137MTrinity Sterile, Inc. · FORCEPS, BIOPSY, GYNECOLOGICAL1 recall0 reports
- AESCULAP ER063RAesculap AG · FORCEPS, BIOPSY, GYNECOLOGICAL2 reports
- Cervical Biopsy Punch 1Dtr Medical Limited · Forceps, Biopsy, Gynecological1 report
- Integra® Miltex® 30-1495Integra Lifesciences Production Corporation · FORCEPS, BIOPSY, GYNECOLOGICAL1 report
- AESCULAP ER064RAesculap AG · FORCEPS, BIOPSY, GYNECOLOGICAL1 report
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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