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. 2,851 recalls have been distributed to California in the last 12 months.
Showing 23821–23840 of 56,506 recalls
Recalled Item: Vigilant Agilia Recalled by Fenwal Inc Due to The firm is correcting four...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VOLUMAT MC AGILIA US Recalled by Fenwal Inc Due to The firm is correcting...
The Issue: The firm is correcting four software anomalies and KVO (keep vein open) end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 Model # 728231 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Model # 728323 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to In certain...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Recalled by Philips Medical Systems (Cleveland) Inc Due to In...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity TF PET/CT Model # 882456 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCT SP Model # 728311 Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Model # 728321 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vereos PET/CT Model # 882446 Recalled by Philips Medical Systems (Cleveland)...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IQon Spectral CT Model # 728332 Recalled by Philips Medical Systems...
The Issue: In certain instances when performing a cardiac step and shoot acquisition...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Recalled by Randox Laboratories, Limited Due to There was a...
The Issue: There was a report of a malfunction with the sensor which resulted in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Imola Recalled by Randox Laboratories, Limited Due to There was a report...
The Issue: There was a report of a malfunction with the sensor which resulted in an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENCONTUSS (Chlorpheniramine Maleate Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dayma SUPER FORTE XL10 (Camphor 0.5% Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg Recalled by Pharma-Natural Inc....
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARMY HEALTH Pain Reliever Gel With CURCUMIN (Menthol 3.00%) Recalled by...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%) Recalled by...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% &...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SORBUGEN NR (Dextromethorphan HBr Recalled by Pharma-Natural Inc. Due to...
The Issue: CGMP Deviations: products were manufactured with lack of process validation,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.