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. 2,669 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,669 in last 12 months

Showing 4182141840 of 56,506 recalls

DrugJune 23, 2015· Actavis Laboratories, FL, Inc.

Recalled Item: Desmopressin Acetate Tablets Recalled by Actavis Laboratories, FL, Inc. Due...

The Issue: Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted...

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

Class III — Low RiskOngoing
Refund
FoodJune 23, 2015· Pinnacle Foods, LLC

Recalled Item: Wish-Bone Ranch Dressing Net. Wt. 24 oz. Distributed by Pinnacle Recalled by...

The Issue: Wishbone Salad Ranch Dressing contains undeclared eggs.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 23, 2015· Pages Produce Company Inc.

Recalled Item: La Mexicana Spinach Dip Net Wt. 14oz. clear Recalled by Pages Produce...

The Issue: Milk is not declared as a sub-ingredient in the declared sour cream.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 23, 2015· O-Two Medical Technologies, Inc.

Recalled Item: O-Two Adult Ventilation Timer Recalled by O-Two Medical Technologies, Inc....

The Issue: Malfunction of an O-Two Adult Ventilation Timer, where the flash rate of the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Draeger Medical, Inc.

Recalled Item: Fabius MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to the...

The Issue: the Fabius MRI or parts of the system were attracted by the magnetic field...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems with software versions...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Volcano Corporation

Recalled Item: Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3...

The Issue: A software issue was discovered where an inaccurate FFR/iFR value could be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2015· Nobel Biocare Usa Llc

Recalled Item: Abutment Retrieval Instrument Zirconia CC RP/WP Recalled by Nobel Biocare...

The Issue: One dimension of the affected instrument is incorrect. Therefore this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJune 19, 2015· Project 7

Recalled Item: Sour Caramel Apple Chewing Recalled by Project 7 Due to Undeclared Milk

The Issue: Project 7 is recalling all lots of Sour Caramel Apple Chewing Gum because...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2015· Atrium Medical Corporation

Recalled Item: Atrium 36Fr Right Angled Firm PVC Thoracic Catheter Recalled by Atrium...

The Issue: Inner pouches incorrectly labeled as part 8136, 36Fr Right Angled...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2015· CooperSurgical, Inc.

Recalled Item: Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Recalled...

The Issue: Incorrect expiration date on outer carton kit label

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 18, 2015· Qualitest Pharmaceuticals

Recalled Item: Disulfiram tablets Recalled by Qualitest Pharmaceuticals Due to Failed...

The Issue: Failed Dissolution Specifications: During routine stability testing at the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 17, 2015· Acon Laboratories, Inc.

Recalled Item: Mission -Breath Alcohol Detector -15 tests - 0.08% BAC - Recalled by Acon...

The Issue: Acon Laboratories, Inc. is recalling Mission Breath Alcohol Detector due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceJune 17, 2015· Philips Electronics North America Corporation

Recalled Item: Invivo Expression MRI Patient Monitoring System. Recalled by Philips...

The Issue: The device's labeling inaccurately indicates Endotracheal as a body...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2015· B. Braun Interventional Systems

Recalled Item: Celsite Implantable Access Port System Recalled by B. Braun Interventional...

The Issue: The manufacturer, B. Braun medical France, received endotoxin test results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2015· Symmetry Surgical, Inc.

Recalled Item: SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP Recalled by Symmetry Surgical, Inc....

The Issue: Lack of sterility assurance.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing