AESCULAP PM408RRecalls & reported problems
Aesculap AG · MARYLAND ADTEC BIPOLAR Grasping Forceps, complete instrument, curved, (310 mm), diam. 5 mm, fenestrated, double action, consisting of PM438R, PM450R, PM973R, reusable · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653322855), received between Nov 12, 2025 and Nov 12, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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
- Break1
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.
InjuryNov 12, 2025Break; Break
ACCORDING TO THE COMPLAINANT DURING A LAPAROSCOPIC PROCEDURE, THE JAW BROKE INSIDE THE PATIENT. PIECE RETRIEVAL WAS COMPLETED SUCCESSFULLY AND X-RAY RESULTS CONFIRMED THIS ALSO. ADDITIONAL INFORMATION WAS NOT PROVIDED BUT HAS BEEN REQUESTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23536101 ↗
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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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