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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2898129000 of 56,506 recalls

Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2018· St Jude Medical Inc.

Recalled Item: Fortify Recalled by St Jude Medical Inc. Due to The firm is releasing new...

The Issue: The firm is releasing new firmware for high voltage implantable cardiac...

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

Class II — Potential Health HazardOngoing
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grand Canyon Foods International LLC.

Recalled Item: Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods Recalled by...

The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Multiple products marketed...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grand Canyon Foods International LLC.

Recalled Item: Southwestern Gourmet Butter Popcorn Grand Canyon Foods Recalled by Grand...

The Issue: An FDA inspection revealed products that contained Yellow 5 and soy lecithin...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Peaceful Mountain -Stomach Rescue - Dietary supplement - Elemental silver...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 16, 2018· Grato Holdings, Inc.

Recalled Item: Peaceful Mountain Recalled by Grato Holdings, Inc. Due to Multiple products...

The Issue: Multiple products marketed as dietary supplements are unapproved new drugs...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 16, 2018· Epic Products, LLC

Recalled Item: Euphoric Premium Male Performance Enhancer capsules Recalled by Epic...

The Issue: Marketed Without An Approved NDA/ANDA: product contains undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 13, 2018· Boiron Inc.

Recalled Item: Calendula Cream Recalled by Boiron Inc. Due to Labeling: Labeling Error on...

The Issue: Labeling: Labeling Error on Declared Strength; The outer carton (secondary...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· Smiths Medical ASD Inc.

Recalled Item: Medfusion Syringe Infusion Pump Recalled by Smiths Medical ASD Inc. Due to...

The Issue: Certain Barrel Clamp Guides may contain a ridge that could potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· TriMed Inc.

Recalled Item: Nitinol Staple Recalled by TriMed Inc. Due to During a retrospective review...

The Issue: During a retrospective review of sterilization records, TriMed has...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· Cardiovascular Systems Inc

Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to The pumps may switch to...

The Issue: The pumps may switch to stand-by during use requiring the pump to be reset...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· St Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS Programmer software model 3330 Recalled by St Jude Medical,...

The Issue: Devices inappropriately displayed a low battery indicator determined to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2018· CareFusion 303, Inc.

Recalled Item: Alaris Pump Recalled by CareFusion 303, Inc. Due to The bezel manufacturing...

The Issue: The bezel manufacturing process for the FR-110 plastic may have resulted in...

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

Class I — Serious Health HazardOngoing
DrugApril 12, 2018· AMA Wholesale

Recalled Item: Rhino 69 Extreme 50000 packaged in 1 capsule per blister pack Recalled by...

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found the product to...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 11, 2018· Premier Pharmacy Labs Inc

Recalled Item: Hydromorphone HCl 1 mg/mL PF INJ. 1mL in a 3mL Recalled by Premier Pharmacy...

The Issue: Lack of Assurance of Sterility:Microbial contamination was detected during...

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

Class II — Potential Health HazardOngoing
Refund