AESCULAP PO777RRecalls & reported problems
Aesculap AG · ADTEC MONOPOLAR Grasping Forceps, jaw inserts, straight, (310 mm), diam. 5 mm, 1 x 1 prong, double action, 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 04046963331351), received between Mar 18, 2021 and Mar 18, 2021 — 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.
Most reported problems
Device problems
- Break1
- Material Twisted/Bent1
Patient problems
- Insufficient Information1
- 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.
InjuryMar 18, 2021Break; Material Twisted/Bent
AN ADDITIONAL MEDICAL INTERVENTION WAS NECESSARY. THIS EVENT PROLONGED THE SURGERY FOR 10-15 MINUTES. THE ADVERSE EVENT IS FILED UNDER AAG REFERENCE XC (B)(4); (B)(4). INVOLVED COMPONENTS: PM973R - INSULATED OUTER TUBE 5/5MM 310MM - LOT UNKNOWN. PO959R - MONOPOLAR HANDLE WITH RATCHET - LOT UNKNOWN.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11517412 ↗
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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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