SOL-M 10ml Oral Dispensing Syringe Clear w/Tip Cap(Gasket type, bulk,non-sterile 21010GCNSBRecalls & reported problems
Sol-Millennium Medical, Inc. · Class 1
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 00810018097929), received between May 16, 2025 and May 16, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Incorrect Measurement” (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
- Incorrect Measurement1
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.
MalfunctionMay 16, 2025Incorrect Measurement; Incorrect Measurement
"PLEASE NOTE THAT ORAL SYRINGES REF# 21010GCNSB FAILED OUR CLIENT FIRST PRODUCTION TESTING DUE TO CAPACITY - VOLUMETRIC OOS, PLEASE SEE DETAILS BELOW: THE SUBMITTED SAMPLE(S) DID NOT MEET THE CAPACITY - VOLUMETRIC REQUIREMENTS FOR THE FOLLOWING: CLAIM: 10 ML, SPEC: MIN: 9.6 ML, ACTUAL TEST RESULTS: 9.4 ML. "
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22035546 ↗
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- NEOMED* BA-S35EOAvanos Medical, Inc. · DISPENSER, LIQUID MEDICATION1 recall0 reports
- NEOMED* BB-S1EOAvanos Medical, Inc. · DISPENSER, LIQUID MEDICATION1 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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