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. 2,656 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,656 in last 12 months

Showing 4378143800 of 56,506 recalls

Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2015· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2015· American Health Packaging

Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 2, 2015· Maquet Cardiovascular Us Sales, Llc

Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...

The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2015· Hill-Rom, Inc.

Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...

The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2015· Baxter Healthcare Corp

Recalled Item: Master Drug Library Software version 8.0 Recalled by Baxter Healthcare Corp...

The Issue: Loading/Bolus default dose settings in the Master Drug Library and the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 27, 2015· Akorn, Inc.

Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...

The Issue: Failed Stability Specifications: Out of specification for preservative,...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2015· AVKARE Inc.

Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
FoodFebruary 27, 2015· Unilever United States, Inc.

Recalled Item: Talenti Gelato & Sorbetto Recalled by Unilever United States, Inc. Due to...

The Issue: Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 27, 2015· Sunshine Burger & Specialty Food Company, LLC

Recalled Item: Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers...

The Issue: Gluten testing was performed on products labeled gluten free. The results...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2015· Sunshine Burger & Specialty Food Company, LLC

Recalled Item: Frozen vegetable-based burgers RETAIL - DOMESTIC: Organic Sunshine Burgers...

The Issue: Gluten testing was performed on products labeled gluten free. The results...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 27, 2015· Sunshine Burger & Specialty Food Company, LLC

Recalled Item: Organic Sunshine Burgers Gluten Free Soy Free Vegan Loco Chipotle Recalled...

The Issue: Gluten testing was performed on products labeled gluten free. The results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 27, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...

The Issue: Stryker received four customer complaints reporting that inside the box...

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugFebruary 26, 2015· Pfizer Inc.

Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 26, 2015· Ethicon Endo-Surgery Inc

Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...

The Issue: During an internal inspection of the production process the firm discovered...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Civco Medical Instruments Inc

Recalled Item: CIVCO Surgi-Tip Transducer Cover Sterile (15.2 x 244 cm) polyethylene...

The Issue: Leaks were detected in the recalled lot which may compromise the sterility...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 26, 2015· Biomet, Inc.

Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...

The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...

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

Class II — Potential Health HazardOngoing