VIDAS® Quality Control 30706Recalls & reported problems
Biomerieux SA · Automated test for use on the VIDAS® system to detect abnormal operation of the VIDAS and mini VIDAS instrument pipette mechanisms and optical systems. · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 1 still open.
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 16, 2026.
Recalls naming this device
- Nov 9, 2022Open, Classified
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Z-0800-2023 · Root cause: Storage · Recall details · FDA record ↗
- Jan 4, 2018Terminated
Increase of events affecting performance regarding pump clogging and displacement of the color-coded SPR label (DOT). These performance issues could contribute to erroneous results for any assay performed on the VIDAS and mini VIDAS system due to a decrease of pipetted volume.
Z-2429-2018 · Root cause: Device Design · Recall details · FDA record ↗
Other Multi-analyte controls unassayed devices
- Multichem ID-B SR103BTechno-Path Manufacturing Limited · Multi-Analyte Controls Unassayed2 recalls0 reports
- QC Sets and Panels: Helix Elite™ 8234Microbiologics Inc. · Multi-analyte controls unassayed2 recalls0 reports
- Helix Elite™ Molecular Standards: Inactivated Standard HE0044NMicrobiologics Inc. · Multi-analyte controls unassayed2 recalls0 reports
- QC Sets and Panels: KWIK-STIK™ 8164Microbiologics Inc. · Multi-analyte controls unassayed2 recalls0 reports
- Multichem IA Plus 08P86-10Techno-Path Manufacturing Limited · Multi-Analyte Controls Unassayed1 recall0 reports
- SEROLOGY I POSITIVE CONTROL (SEROLOGY I CONTROL +) SR10352Randox Laboratories Limited · Multi-Analyte Controls Unassayed1 recall0 reports
- Multichem S Plus 08P88-12Techno-Path Manufacturing Limited · Multi-Analyte Controls Unassayed1 recall0 reports
- Helix Elite™ Molecular Standards: Inactivated Standard HE0070NMicrobiologics Inc. · Multi-Analyte Controls Unassayed1 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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