MEDI-VAC 65652-631ARecalls & reported problems
Cardinal Health 200, LLC · CRD Flex 3000cc Canister W/Valve · Class 2
All models of MEDI-VAC (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 1
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 50885380158610), received between Aug 28, 2020 and Aug 28, 2020 — classified as 1 death.
The most frequently reported specific device problem is “Suction Problem” (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
- Suction Problem1
- Use of Device Problem1
Patient problems
- Cardiac Arrest1
- Death1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
DeathAug 28, 2020Use of Device Problem; Suction Problem; Suction Problem
THE SUCTION CANISTER IS USED WITHOUT A STAND KEEPING IT VERTICAL AND CAN BE LYING DOWN OR SHOCKED AT ANY TIME DURING RESUSCITATION. THIS MAY RESULT IN THE SAFETY VALVE BEING CLAMPED ON THE OUTLET AND THEREBY STOPPING THE SUCTION. LACK OF INFORMATION ON THE DEVICE, ON THE RISK OF STOPPING THE VACUUM. THIS TYPE OF EVENT WAS SUSPECTED DURING LOSS OF SUCTION DURING CPR (CARDIOPULMONARY RESUSCITATION) IN EMERGENCIES, HAVING RESULTED IN EIGAS (SERIOUS ADVERSE EVENT RELATED TO TREATMENT) DEATH OF PATIENT.
Patient problems: Cardiac Arrest; Death
MAUDE report 10468687 ↗
Other APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED devices
- StrykeFlow 0250070520Stryker Corporation · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED2 recalls250 reports
- StrykeFlow 0250070505Stryker Corporation · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall3 reports
- Sentinel Seal 8888571562Cardinal Health 200, LLC · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall0 reports
- Aqua-Seal 8888571299Cardinal Health 200, LLC · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall0 reports
- spineX BONE DUST COLLECTOR S-4500Oto-Med, Inc. · Apparatus, Suction, Operating-Room, Wall Vacuum Powered1 recall0 reports
- Aqua-Seal 8888571406Cardinal Health 200, LLC · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall0 reports
- Altitude 8888571370Cardinal Health 200, LLC · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall0 reports
- CRD 65651-517Cardinal Health 200, LLC · APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1 recall0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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