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. 2,867 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,867 in last 12 months

Showing 2194121960 of 56,506 recalls

DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: R2103 Recalled by Washington Homeopathic Products, Inc. Due to CGMP...

The Issue: CGMP Deviations: products were not manufactured under current good...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Natrum Phosphoricum 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Natrum Muriaticum 6X Tablets Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 8, 2019· Washington Homeopathic Products, Inc.

Recalled Item: Pareira (Brava) 1X Tincture Recalled by Washington Homeopathic Products,...

The Issue: CGMP Deviations: products were not manufactured under current good...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Cook Inc.

Recalled Item: CrossCath Support Catheter Recalled by Cook Inc. Due to A manufacturing...

The Issue: A manufacturing error may cause the radiopaque marker bands to be too loose...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceNovember 8, 2019· Boston Scientific Corporation

Recalled Item: AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D 105650-001H...

The Issue: Missing Directions for Use (DFU) - Consoles shipped to customers without the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: Beckman Coulter has become aware of an issue affecting Specific Gravity...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Ethicon Endo-Surgery Inc

Recalled Item: Ligamax 5 mm Endoscopic Multiple Clip Applier Recalled by Ethicon...

The Issue: A potential exists that certain LIGAMAX devices within the impacted lots may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Abbott Gmbh & Co. KG

Recalled Item: ARCHITECT HAVAB-G Calibrator Recalled by Abbott Gmbh & Co. KG Due to Abbott...

The Issue: Abbott has identified that Calibrator lot 08219BE00 is potentially impacted...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Neuronetrix Solutions, LLC dba Cognision

Recalled Item: Cognision Recalled by Neuronetrix Solutions, LLC dba Cognision Due to...

The Issue: Product has the potential to be contaminated with Burkholderia cepacia (B....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2019· Howmedica Osteonics Corp.

Recalled Item: Stryker Omnifit Crossfire 10 Degree Series II Insert- intended for Recalled...

The Issue: May have a missing locking wire causing delay in surgery while retrieving a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodNovember 7, 2019· Gold Standard Baking, Inc.

Recalled Item: Freshness Guaranteed Croissants in clear plastic 12oz clamshell Recalled by...

The Issue: Product is missing ingredient and nutrition label on bottom of clamshell...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution Recalled by AuroMedics Pharma LLC...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Caspules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: DG Health Acid Reducer Ranitidine Tablets 150 mg Recalled by AuroMedics...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 300 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2019· AuroMedics Pharma LLC

Recalled Item: Aurobindo Ranitidine Capsules 150 mg Recalled by AuroMedics Pharma LLC Due...

The Issue: CGMP Deviations: N-nitrosodimethylamine (NDMA) has been detected in...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund