Bovie SERFRecalls & reported problems
Aspen Surgical Products, Inc. · REDUCER FITTING 7/8" (2.22cm) TO ¼" (.63cm) X WITH ¼" (.63cm) X 24” (60.96CM) MEDICAL (PVC) TUBING (10 PER POUCH) · Class 2
All models of Bovie (42)
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 00607151001667), received between May 11, 2022 and May 11, 2022 — classified as 1 malfunction.
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
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 11, 2022Break
THE ONLY INFORMATION RECEIVED WAS MAUDE WATCH REPORT THAT STATES THAT THERE WAS A POSSIBLE INJURY THAT REQUIRED INTERVENTION. THE EVEN DESCRIPTION WAS "BREAK" .
Patient problems: Unspecified Tissue Injury
MAUDE report 14361936 ↗
Other Tubing, Noninvasive devices
- Argyle 8888301614Cardinal Health, Inc. · TUBING, NONINVASIVE14 reports
- Argyle 8888301713Cardinal Health, Inc. · TUBING, NONINVASIVE11 reports
- Argyle 5558301627Cardinal Health, Inc. · TUBING, NONINVASIVE3 reports
- MEDLINE DYND50252Medline Industries, Inc. · TUBING, NONINVASIVE3 reports
- Argyle 8888301523Cardinal Health, Inc. · TUBING, NONINVASIVE3 reports
- MEDLINE DYND50251Medline Industries, Inc. · TUBING, NONINVASIVE2 reports
- Argyle 8888301606Cardinal Health, Inc. · TUBING, NONINVASIVE2 reports
- NA SVT-089Boston Scientific Corporation · TUBING, NONINVASIVE2 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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