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. 3,068 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,068 in last 12 months

Showing 28012820 of 13,703 recalls

DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: MILK OF MAGNESIA USP Recalled by Plastikon Healthcare LLC Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: CORRECTDOSE Children's ALLERGY RELIEF (Diphenhydramine HCl 12.5 mg per 5 mL)...

The Issue: CGMP Deviations: products manufactured under conditions which manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: MILK OF MAGNESIA USP Recalled by Plastikon Healthcare LLC Due to CGMP...

The Issue: CGMP Deviations: products manufactured under conditions which manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: CORRECTDOSE Children's COUGH & CHEST CONGESTION DM (Guaifenesin 100 mg...

The Issue: CGMP Deviations: products manufactured under conditions which manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL Recalled by Plastikon...

The Issue: CGMP Deviations: products manufactured under conditions which manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: Magnesium Hydroxide 2400 mg Recalled by Plastikon Healthcare LLC Due to...

The Issue: Microbial Contamination of Non-Sterile Products.

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 7, 2022· Plastikon Healthcare LLC

Recalled Item: GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL Recalled by Plastikon...

The Issue: CGMP Deviations: products manufactured under conditions which manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2022· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets Recalled by PD-Rx Pharmaceuticals, Inc. Due to...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: Manufacturing deviations were reported due to an abnormal...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2022· Akorn, Inc.

Recalled Item: Olopatadine HCl Recalled by Akorn, Inc. Due to Failed impurity/degradation...

The Issue: Failed impurity/degradation specifications: Out of specification for 2-HMP...

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

Class III — Low RiskOngoing
Refund
DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: CGMP Deviations: lots made with same active pharmaceutical ingredient (API)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 3, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Clonazepam Orally Disintegrating Tablets Recalled by SUN PHARMACEUTICAL...

The Issue: Failed Tablet/Capsule Specification; oversized tablet found in a bottle

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...

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

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 24, 2022· Grato Holdings, Inc.

Recalled Item: Homeopathic EarAche Drops Recalled by Grato Holdings, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri Ajo King con Ortiga y Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2022· Walmart Inc

Recalled Item: Artri King con Ortiga Omega 3 Tablets Recalled by Walmart Inc Due to...

The Issue: Marketed Without An Unapproved NDA/ANDA: All lots were found to be...

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

Class II — Potential Health HazardOngoing
Refund