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Pharmaceutical Innovations Recalls
6 recalls on record · July 24, 2019 to August 26, 2020 · Medical Devices
Recalls by year
19
20
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
August 26, 2020Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls Ultra/Phonic Focus BP Conforming Gel Pads, UDI 00300361301021 (Primary); 10300361301028 (Package) - Product Usage: A gel
Hazard: The firm registered the product as a Class I device, but has since been informed by FDA that the device is not Class I and requires a 510(k) submission.
July 24, 2019Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
Hazard: Potential for failed stability antimicrobial effectiveness testing.
July 24, 2019Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls ElectroMist product codes: 36-3310-04 - Product Usage: Electrode Conductivity Spray Solution.
Hazard: Potential for failed stability antimicrobial effectiveness testing.
July 24, 2019Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.
Hazard: Potential for failed stability antimicrobial effectiveness testing.
July 24, 2019Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
Hazard: Potential for failed stability antimicrobial effectiveness testing.
July 24, 2019Medical DevicesFDA
Pharmaceutical Innovations, Inc. recalls Alpha Conducting solution product codes:3310-15 ACS - Product Usage: Electrode conductivity spray solution.
Hazard: Potential for failed stability antimicrobial effectiveness testing.