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. 3,026 recalls have been distributed to California in the last 12 months.

56,506 total recalls
3,026 in last 12 months

Showing 80418060 of 13,703 recalls

DrugJune 8, 2017· Phillips Co.

Recalled Item: TetraStem brand Topical Ointment First Aid Antibiotic Recalled by Phillips...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: StingMed Insect bites Skin Protectant. Zinc acetate (.1% by volume) Recalled...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: StaphWash+Plus+ Skin Protectant Recalled by Phillips Co. Due to GMP...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 8, 2017· Phillips Co.

Recalled Item: Tetracycline-ABC Brand Topical ointment First Aid Antibiotic Recalled by...

The Issue: GMP Deviations; FDA inspection found significant manufacturing practices...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 6, 2017· Bausch & Lomb, Inc.

Recalled Item: NasalCrom (cromolyn sodium) Nasal Spray Recalled by Bausch & Lomb, Inc. Due...

The Issue: CGMP Deviations: Possibility of the presence of microbial contamination in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 5, 2017· Bristol-myers Squibb Company

Recalled Item: EliquisTablets 5mg Recalled by Bristol-myers Squibb Company Due to Labeling:...

The Issue: Labeling: Label Mix-up: One bottle of Eliquis 5 mg tablet was found to...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 5, 2017· Apothecary By Design

Recalled Item: Progesterone Injection in Olive Oil With Benzyl Alcohol 10% Recalled by...

The Issue: Lack of Processing Controls: The metal container closure adheres to the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2017· G & W Laboratories, Inc.

Recalled Item: G & W Clobetasol Propionate Ointment 0.05% Recalled by G & W Laboratories,...

The Issue: Failed impurities/degradation specifications: This product is being recalled...

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

Class III — Low RiskOngoing
Refund
DrugJune 1, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...

The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· Lucid Pharma LLC

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...

The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· L. Perrigo Company

Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...

The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2017· Teva Pharmaceuticals

Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...

The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

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

Class III — Low RiskOngoing
Refund
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Capsules Recalled by Shionogi Inc. Due to Presence of foreign...

The Issue: Presence of foreign substance: The recall was initiated due to black...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugMay 24, 2017· Shionogi Inc.

Recalled Item: Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Low dissolution results were obtained...

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

Class III — Low RiskOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 22, 2017· Dr. Reddy's Laboratories, Inc.

Recalled Item: Zenatane (isotretinoin) Capsules Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed Dissolution Specifications: out of specification results observed for...

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

Class II — Potential Health HazardOngoing
Refund