Product Recalls in California
Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 3,026 recalls have been distributed to California in the last 12 months.
Showing 8921–8940 of 30,923 recalls
Recalled Item: Conductivity Sensors utilized on Dialog and Dialog+ Hemodialysis Systems....
The Issue: Firm learned of the potential for cracks to form in the conductivity sensors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus LS Recalled by Remote Diagnostic Technologies Ltd. Due to...
The Issue: Distribution of Defibrillators that are not approved or cleared for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material #...
The Issue: Dimension Vista Magnesium Flex reagent cartridge lots exhibiting imprecision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAM CHEST SEAL Combo LOT Y060321-09 Recalled by Sam Medical Products Due to...
The Issue: Due to partially assembled valved dressing that has a hole within it instead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESCAPE Central Station (CSCS) V2.0x MAI700 (Integrated)...
The Issue: If the CARESCAPE Central Station v2.0 is used with an unapproved keyboard,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brasseler USA Recalled by Brasseler USA, Medical L.L.C. Due to One lot of...
The Issue: One lot of product was distributed in unsealed packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G: MMT-1715 Recalled by Medtronic MiniMed Due to New or...
The Issue: New or replacement insulin pumps are not pre-programmed with basal rates or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Extraction Reagent-X Recalled by Hologic, Inc Due to Failed...
The Issue: Failed stability specifications for reagent kits that may result in false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...
The Issue: There is a potential to leak from the catheter where it connects to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SURESTEP INTERMITTENT CATHETER TRAY Recalled by C.R. Bard Inc Due to...
The Issue: There is a potential to leak from the catheter where it connects to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...
The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Matrix Clinical Solution At-Home COVID-19 Test Recalled by Matrix Medical...
The Issue: Due to COVID-19 Test not being authorized for home sample collection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntraSight Mobile IVUS Systems Recalled by Volcano Corp Due to...
The Issue: Multi-Modality Touch Screen Modules (MM-TSM), which are bedside/secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1138747 Recalled by...
The Issue: A limited number of ventilators were assembled with expired adhesive. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 Recalled by...
The Issue: A limited number of ventilators were assembled with expired adhesive. If the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recalled by...
The Issue: Guidewire included with two lots of Arterial Line Kits would not fit through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.