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. 1,074 recalls have been distributed to California in the last 12 months.
Showing 35161–35180 of 56,506 recalls
Recalled Item: Halyard C-Section Drape with Clear Screen and Full Incise (Non-Sterile)...
The Issue: Drapes within the affected lots may include a manufacturing variation that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Regular Set Wash Material Recalled by Ivoclar...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: L-Cysteine Hydrochloride Injection Recalled by Sandoz Inc Due to Lack of...
The Issue: Lack of Assurance of Sterility: a recent FDA inspection at the manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactulose Solution Recalled by VistaPharm, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: bulk solution tested...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Techni-Care Surgical Hand Scrub and Patient Preoperative Skin Preparation...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date - Product is missing or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARROW OnControl Bone Lesion Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Ported Aspiration System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Tray Recalled by Teleflex Medical...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREMIER EHEC and PREMIER EHEC Bulk. Recalled by Meridian Bioscience Inc Due...
The Issue: Internal testing has demonstrated that the indicated kit lots produce false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OnControl Biopsy System Ported Needle Tray Recalled by Teleflex Medical Due...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW OnControl Bone Marrow Biopsy System Comprehensive Tray Recalled by...
The Issue: Sterility: Due to a potential incomplete seal on the outer sterile package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Performance-LOAD Ambulance Cot Fastener Stretcher Recalled by Stryker...
The Issue: Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CANNIBAL FEROX AMPED Recalled by Chaos and Pain Due to Product was analyzed...
The Issue: Product was analyzed and found to contain 1,3- dimethylbutylamine which was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cucumber Recalled by Prime Time International Due to Potential Salmonella...
The Issue: Prime Time is recalling cucumber bushels because they have the potential to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase...
The Issue: Due to a customer experiencing complaints on bone fraction of assay not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Hemotherm 400CE 115v Recalled by Cincinnati Sub-Zero Products Inc Due to...
The Issue: The device may not maintain water flow or temperature control.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alteon Neck Preserving Stem Recalled by Exactech, Inc. Due to Products were...
The Issue: Products were labeled with incorrect Global Trade Item Numbers. The GTIN on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing. Recalled by Tosoh...
The Issue: The device defect associated with this recall may result in HbA1c values...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.