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. 2,669 recalls have been distributed to California in the last 12 months.
Showing 41281–41300 of 56,506 recalls
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7 Hole VL Gridlock Fibula Plate Recalled by Trilliant Surgical Ltd. Due to...
The Issue: The affected parts subject to the recall are out of specification, resulting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR"* 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Triple Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar" Elite Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...
The Issue: Sterility may be compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Guide Recalled by Tornier, Inc Due to Tornier has...
The Issue: Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Topicort (desoximetasone) Topical Spray Recalled by Taro Pharmaceuticals,...
The Issue: Failed Impurities/Degradation Specifications: Out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy Recalled by...
The Issue: The neoBLUE Instruction For Use (IFU) and Service Manuals for the neoBLUE 3...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTISTE Recalled by Siemens Medical Solutions USA, Inc Due to A software fix...
The Issue: A software fix has been released to prevent automatic movement resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology...
The Issue: The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Parsippany Recalled by Biomet Spine, LLC Due to Mislabeling
The Issue: Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExacTrac 6.0.x Patient Positioning System Recalled by Brainlab AG Due to...
The Issue: ExacTrac 6.0 Patient Positioning System: Display of potentially incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expello-C packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs...
The Issue: The powdered golden seal had a coliform count of 2000 cfu/g when the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: A&W Cream Soda 12 FL OZ (355 mL) Recalled by Dr. Pepper Snapple Group Inc...
The Issue: The American Bottling Company is recalling 12 oz. cans of A& W Cream Soda...
Recommended Action: Do not consume. Return to store for a refund or discard.