SSCOR VX-2® 2310BVRecalls & reported problems
Sscor, Inc. · Portable Suction Device · Class 2
- Adverse event reports
- 10
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI B2452310BV0), received between Mar 20, 2019 and Nov 19, 2025 — classified as 10 malfunctions.
The most frequently reported specific device problem is “Premature Discharge of Battery” (5 reports).
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.
Reports received per month
Most reported problems
Device problems
- Premature Discharge of Battery5
- Battery Problem3
- Electrical /Electronic Property Problem1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions9
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 10 most recent of 10 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2025Battery Problem; Battery Problem
(B)(6) AMBULANCE SERVICES REPORTED THAT A VEHICLE FELL ON ADULT MALE IN A GARAGE, PATIENT HAD EMESIS IN AIRWAY, SUCTION UNIT BLINKED RED WHEN ATTEMPTING TO BE USED, BACK UP SUCTION UNIT WAS USED INSTEAD. ULTIMATELY THE SUCTION DEVICE DID NOT CONTRIBUTE TO THE PATIENT OUTCOME. WHEN ASKED IF THEY WOULD SEND THE DEVICE IN FOR EVAL, THEY REQUIRED A LOANER DEVICE. REPLACEMENT BATTERY WAS ISSUED AND THIS RESOLVED THEIR ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23594851 ↗MalfunctionMar 24, 2025Battery Problem; Battery Problem
ON (B)(6) 2025 (B)(6) FIRE DEPT. REPORTED THAT DEVICE SN (B)(6) DIED AT THE END OF AN CARDIAC ARREST CALL. DEVICE DIED WITH IN 30 MINUTES INTO THE CALL AS FAR AS TO WHEN VOLUNTEER WENT TO DO INTUBATION. REPORTED STATED THAT DEVICE IS ALWAYS KEPT ON CHARGE. SSCOR ISSUED A REPLACEMENT BATTERY TO RESOLVE THEIR ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21684453 ↗MalfunctionMay 16, 2024Premature Discharge of Battery; Premature Discharge of Battery
BATTERY FAILURE, UNIT DID NOT HOLD A CHARGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19337720 ↗MalfunctionMay 16, 2024Premature Discharge of Battery; Premature Discharge of Battery
BATTERY FAILURE, UNIT DID NOT HOLD A CHARGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19337715 ↗MalfunctionMay 16, 2024Premature Discharge of Battery; Premature Discharge of Battery
BATTERY FAILURE, UNIT DID NOT HOLD A CHARGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19337713 ↗MalfunctionJul 13, 2023Electrical /Electronic Property Problem; Electrical /Electronic Property Problem
BATTERY FAILED DURING A CARDIAC ARREST CALL. DEVICE STOPPED WORKING WITH IN TWO MINUTES INTO THE CALL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17322039 ↗MalfunctionJul 13, 2023Battery Problem; Battery Problem
BATTERY FAILED DURING A CARDIAC ARREST CALL. UNIT WILL TURN ON BUT THERE WAS NOT ENOUGH SUCTION. SSCORT III WAS USED AS BACK UP.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17321817 ↗MalfunctionMay 19, 2023Premature Discharge of Battery; Premature Discharge of Battery
DURING A CARDIAC ARREST CALL DEVICE TURNED ON BUT DIED WITH IN 20 SECONDS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16967314 ↗MalfunctionJan 23, 2023Premature Discharge of Battery; Premature Discharge of Battery
MEDIC UNIT WAS RESPONDING TO A CALL FOR CARDIAC PROBLEM. DURING INTUBATION DEVICE WAS UNABLE TO SUCTION AND MEDIC UNIT HAD TO WAIT FOR A WORKING UNIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16230242 ↗MalfunctionMar 20, 2019No Apparent Adverse Event; No Apparent Adverse Event
"WE HAD A PATIENT IN CARDIAC ARREST WHO HAD A LOT OF BLOOD IN HIS MOUTH. WE ATTEMPTED TO SUCTION USING THE VX-2, DEVICE WAS ON WITH PUMP RUNNING, THE BATTERY WAS FULLY CHARGED BUT WE COULD NOT GET IT TO SUCTION. THE DEVICE WAS RETURNED TO SUPPLY SO I DO NOT KNOW WHERE IT IS NOW OR IF IT IS BEING REPAIRED OR LOOKED AT. I CAN FORWARD YOUR CONTACT INFORMATION TO SOMEONE WHO MAY BE ABLE TO HELP YOU GET MORE INFORMATION ON THE DEVICE. I AM NOT SURE WHAT THE OUTCOME OF THE PATIENT WAS. I DO NOT THINK HE MADE IT AS HE WAS AN OLDER GENTLEMAN. WE WERE ABLE TO GET A SECOND SUCTION DEVICE. THE DEVICE FAILURE DELAYED THE ABILITY TO PROPERLY VENTILATE HIM, BUT I CAN SAY THAT IT WOULDN'T HAVE MADE A DIFFERENCE. PATIENT HAD A LOT OF PAST MEDICAL CONDITIONS."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8438671 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.