Mityvac 10022Recalls & reported problems
Coopersurgical, Inc. · Reusable Obstetrical Vacuum Pump · Class 2
- 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 00888937003147), received between Dec 4, 2020 and Dec 4, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Deflate” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Failure to Deflate1
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.
MalfunctionDec 4, 2020Failure to Deflate
Other Extractor, Vacuum, Fetal devices
- Kiwi® OmniCup® VAC-6000MTEClinical Innovations, LLC · Extractor, Vacuum, Fetal1 recall1 death20 reports
- Kiwi® OmniCup® VAC-6000MTClinical Innovations, LLC · Extractor, Vacuum, Fetal1 recall1 death7 reports
- Mystic 10057Coopersurgical, Inc. · Extractor, Vacuum, Fetal19 reports
- Kiwi® OmniCup® VAC-6000MClinical Innovations, LLC · Extractor, Vacuum, Fetal14 reports
- Kiwi® OmniCup® VAC-6000MEClinical Innovations, LLC · Extractor, Vacuum, Fetal10 reports
- MityOne 10067Coopersurgical, Inc. · Extractor, Vacuum, Fetal10 reports
- Mityvac 10137Coopersurgical, Inc. · Extractor, Vacuum, Fetal4 reports
- Kiwi® ProCup® VAC-6000SClinical Innovations, LLC · Extractor, Vacuum, Fetal3 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.