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. 1,075 recalls have been distributed to California in the last 12 months.
Showing 30761–30780 of 56,506 recalls
Recalled Item: Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axiom Artis model Interventional fluoroscopic x-ray foot switch accessory...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magstim Rapid Therapy System consisting of: Rapid Mainframe Recalled by The...
The Issue: Users manuals not supplied with 4800-00T US Rapid Therapy System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) Recalled...
The Issue: Correction to update sterilizer software to prohibit the use of expired...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q and Q.zen model Interventional fluoroscopic x-ray system wireless...
The Issue: The possibility exists for the wireless foot switch to fail due to impacts...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lorazepam Tablets Recalled by Leading Pharma, LLC Due to Labeling: Label...
The Issue: Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer performs three methods of...
The Issue: The firm has become aware of a potential issue that may affect the mixing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Recalled...
The Issue: There have been reported incidents of fluid leaks at the luer connection....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glutamine Recalled by United Pharmacy Due to CGMP Deviations; FDA analysis...
The Issue: CGMP Deviations; FDA analysis deterrmined that the product does not contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 2 mL Total Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine HCL 100 mcg per mL (1 mg/10 mL) in Recalled by Pharmedium...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine Sulfate in 0.9% Sodium Chloride Injection 1 mL Total Volume 2 mg...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Tablets Recalled by The Harvard Drug Group Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCl in 0.9% Sodium Chloride Injection Recalled by Pharmedium...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp. Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AIRO Mobile CT System Recalled by Mobius Imaging, LLC Due to If the...
The Issue: If the tilt-drive motor has an intermittent connection or broken encoder or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Footswitch accessory to the CUSA Clarity Ultrasonic Tissue Ablation System...
The Issue: A faulty footswitch may result in unintended ultrasonic fragmentation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Recalled...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Yellow Medication Cassette Reservoir with clamp and female Luer....
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD(TM) Medication Cassette Reservoir with clamp and female Luer. Nonvented...
The Issue: Smiths Medical became aware that certain Non Flow-Stop CADD(R) Medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instant Reishi Coffee Recalled by Chun Yuen Trading Co., Inc. Due to Milk is...
The Issue: Milk is not declared on the product labeling.
Recommended Action: Do not consume. Return to store for a refund or discard.