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.
Showing 29241–29260 of 56,506 recalls
Recalled Item: Conzerol (antipoxin) H2O2 Gel Recalled by Elroselabs Inc. Due to cGMP Deviations
The Issue: cGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ignite High Endurance Pre-Workout Supplement with Caffeine Recalled by...
The Issue: Ignite High Endurance Pre-Workout Supplement with Caffeine dietary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ignite High Endurance Pre-Workout Supplement VANILLA Recalled by Independent...
The Issue: Ignite High Endurance Pre-Workout Supplement VANILLA dietary supplement...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ignite High Endurance Pre-Workout Supplement CAFFEINE FREE Formula Recalled...
The Issue: Ignite High Endurance Pre-Workout Supplement Caffeine Free dietary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ignite High Endurance Pre-Workout Supplement Recalled by Independent...
The Issue: Ignite High Endurance Pre-Workout Supplement dietary supplement product is...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enduravol Elite Pre-Workout Recalled by Independent Nutrition, Inc. Due to...
The Issue: Enduravol Elite Pre-Workout dietary supplement product is recalled because...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: The dose calculation accuracy may in some situations be less than expected....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...
The Issue: Software anomaly resulting in the loss of patient settings and stored...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Blade Shoe F/Unigraft Knife 1.5 Thick X 9MM SKU Recalled by Ace...
The Issue: The product inside the package is incorrect. A single blade shoe was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.54% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.82% Sodium Chloride Injection Recalled by AuroMedics...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin in 5% Dextrose Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Lack of Assurance of Sterility; confirmed customer report of a leaking bags...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.