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. 2,881 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,881 in last 12 months

Showing 2086120880 of 56,506 recalls

DrugFebruary 27, 2020· The Harvard Drug Group

Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2020· Pfizer Inc.

Recalled Item: Elelyso (taliglucerase alfa) for injection Recalled by Pfizer Inc. Due to...

The Issue: Lack of Assurance of Sterility--Reports of loose metal ferrule crimps on...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 26, 2020· Philips North America, LLC

Recalled Item: HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A...

The Issue: Philips has received a number of reports of HeartStart MRx...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2020· Capso Vision, Inc.

Recalled Item: The CapsoCam Plus (SV-3) Recalled by Capso Vision, Inc. Due to Ingestible...

The Issue: Ingestible video capsule system has capsule with incorrect capture mode...

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

Class II — Potential Health HazardOngoing
FoodFebruary 26, 2020· Choice Products LLC.

Recalled Item: Premiere Choice 3lb. Peanut Butter Cookie Dough Recalled by Choice Products...

The Issue: Peanut Butter Cookie Dough may contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 25, 2020· International Food Products Corporation

Recalled Item: Dairy House Ingredients Systems Recalled by International Food Products...

The Issue: The firm received an ingredient that may have been contaminated with metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 25, 2020· International Food Products Corporation

Recalled Item: Dairy House Ingredients Systems Recalled by International Food Products...

The Issue: The firm received an ingredient that may have been contaminated with metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 25, 2020· International Food Products Corporation

Recalled Item: Profile Food Ingredients Recalled by International Food Products Corporation...

The Issue: The firm received an ingredient that may have been contaminated with metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 25, 2020· Driscoll's Inc.

Recalled Item: Driscoll's Blackberries Recalled by Driscoll's Inc. Due to Testing found...

The Issue: Testing found Acephate of 2.8ppm on fresh blackberries. There is no US MRL...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Rhythm Xience Guider Catheter Introducer with Lancer Intergrated...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2020· Kerr/Pentron, DBA Kerr Corporation and Pentron Clinical

Recalled Item: Nexus Universal with OptiBond Universal Recalled by Kerr/Pentron, DBA Kerr...

The Issue: An issue within production process used to package trial kits let to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Acutus Medical AcQGuide Mini Fixed-Curve Introducer with AcQCros QX...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Rhythm Xience Flextra Steerable Introducer with Lancer Integrated...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2020· Acutus Medical Inc

Recalled Item: Acutus Medical AcQGuide Flex Steerable Introducer with AcQcross QX...

The Issue: It has been determined that the manufacturing process may have left foreign...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· LivaNova USA Inc.

Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...

The Issue: The firm is providing validated cleaning and disinfection instructions in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· Butterfly Network, Inc.

Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...

The Issue: Distributed without an approved 510(k)

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2020· Butterfly Network, Inc.

Recalled Item: Butterfly iQ Ultrasound System Auto Bladder Volume Tool-The Auto Bladder...

The Issue: Distributed without an approved 510(k)

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

Class II — Potential Health HazardOngoing
DrugFebruary 24, 2020· Breckenridge Pharmaceutical, Inc

Recalled Item: Zoledronic Acid Injection 5 mg/100 mL (0.05 mg/mL) Recalled by Breckenridge...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 24, 2020· Tova Industries Inc

Recalled Item: Good Source brand Chicken Flavored Rice Meal Recalled by Tova Industries Inc...

The Issue: Downstream recall from supplier. Possible metal shavings in ingredient.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 24, 2020· Tova Industries Inc

Recalled Item: American Bounty brand Soup Base Beef No MSG Recalled by Tova Industries Inc...

The Issue: Downstream recall from supplier. Possible metal shavings in ingredient.

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

Class II — Potential Health HazardOngoing
Refund