Aspirator 798-0330-01Recalls & reported problems
Zoll Medical Corporation · ASSEMBLY, FINAL, M330 ASPIRATOR · Class 2
Data updated Oct 18, 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 00847946023386), received between Sep 22, 2026 and Sep 22, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Battery 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.
Reports received per month
Most reported problems
Device problems
- Battery Problem1
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.
MalfunctionSep 22, 2026Battery Problem
COMPLAINANT ALLEGED THAT DURING BIOMED TESTING, THE DEVICE'S BATTERY VENTED INSIDE THE DEVICE.COMPLAINANT INDICATED THAT THERE WAS NO PATIENT INVOLVEMENT IN THE REPORTED MALFUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50858248 ↗
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- SSCOR VX-2® 2310BVSscor, Inc. · Pump, Portable, Aspiration (Manual Or Powered)10 reports
- CARE-E-VAC 3Ohio Medical, LLC · Pump, Portable, Aspiration (Manual Or Powered)8 reports
- Thopaz+Medela AG · Pump, Portable, Aspiration (Manual Or Powered)2 reports
- Precision Medical Inc. PM65HGPrecision Medical, Inc. · Pump, Portable, Aspiration (Manual Or Powered)1 report
- HAEMONETICS SMARTSUCTION TECHNOLOGY HAR-A-1000Haemonetics Corporation · Pump, Portable, Aspiration (Manual Or Powered)1 report
- Thoraguard FGN-1387Centese, Inc. · Pump, Portable, Aspiration (Manual Or Powered)1 report
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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