Synchron® CX/LX/DX B-Hydroxybutyrate LiquiColor® B2440-180Recalls & reported problems
Stanbio Laboratory, L.P. · For the Quantitative Determination of ß-Hydroxybutyrate in Serum or Plasma. · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier.
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.
Recalls naming this device
- Jul 12, 2021Class IIITerminated
Deterioration in the stability of the reagents which has resulted in lower than expected or out of range Quality Control values.
Z-2201-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other Nitroprusside, Ketones (Urinary, Non-Quant.) devices
- B-Hydroxybutyrate LiquiColor® 2440-058Stanbio Laboratory, L.P. · Nitroprusside, Ketones (Urinary, Non-Quant.)2 recalls0 reports
- CARDINAL HEALTH CH2440058Cardinal Health 200, LLC · NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)1 recall0 reports
- CARDINAL HEALTH CHB2440180Cardinal Health 200, LLC · NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)1 recall0 reports
- One+Step Ketone 81A4Dfi CO.,Ltd · Nitroprusside, Ketones (Urinary, Non-Quant.)1 recall0 reports
- STAT-Site M B-HB Strips 401010Stanbio Laboratory, L.P. · Nitroprusside, Ketones (Urinary, Non-Quant.)1 recall0 reports
- TRUEplus TRUEplus Ketone Test StripsTrividia Health, Inc. · Nitroprusside, Ketones (Urinary, Non-Quant.)33 reports
- Nova Max PlusNova Biomedical Corporation · NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)28 reports
- Precision Xceed Pro 70932Abbott Diabetes Care Inc · NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.)24 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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