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. 2,662 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,662 in last 12 months

Showing 4264142660 of 56,506 recalls

FoodApril 30, 2015· Regency Group, Inc., The

Recalled Item: Fresca Tomato Spice with Beet Recalled by Regency Group, Inc., The Due to...

The Issue: Fresca Tomato Spice with Beet is recalled due to contamination with gluten...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 30, 2015· Regency Group, Inc., The

Recalled Item: French Fry Seasoning Recalled by Regency Group, Inc., The Due to French Fry...

The Issue: French Fry Seasoning is recalled due to contamination with gluten (wheat...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 30, 2015· Regency Group, Inc., The

Recalled Item: Taco Seasoning No Salt Recalled by Regency Group, Inc., The Due to Taco...

The Issue: Taco Seasoning No Salt is recalled due to contamination with gluten (wheat...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 30, 2015· Regency Group, Inc., The

Recalled Item: Turtle Island Roast Beef Spice Blend Recalled by Regency Group, Inc., The...

The Issue: Turtle Island Roast Beef Spice Blend is recalled due to contamination with...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 30, 2015· Regency Group, Inc., The

Recalled Item: Pizza Seasoning Recalled by Regency Group, Inc., The Due to Pizza Seasoning...

The Issue: Pizza Seasoning is recalled due to contamination with gluten (wheat...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 30, 2015· Zimmer, Inc.

Recalled Item: PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual...

The Issue: Potential for uncured adhesive between the metal threaded insert and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2015· Neuro Kinetics, Inc.

Recalled Item: I-Portal¿ NOTC and VNG Recalled by Neuro Kinetics, Inc. Due to complaints of...

The Issue: complaints of system malfunction and unintended, sudden movement at start...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2015· Smith & Nephew, Inc.

Recalled Item: ULTRA-FAST FIX Knot Pusher Suture Cutters Product Number: 72201537 Intended...

The Issue: Sterility of device maybe compromised

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

Class II — Potential Health HazardOngoing
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit Recalled by Mission...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2015· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 9% and Sulfur 4.5% Wash Kit with Sunscreen Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product failed USP...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2015· Janssen Pharmaceuticals, Inc.

Recalled Item: Ortho-Cept (0.15 mg desogestrel and 0.03 mg ethinyl estradiol) tablets...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: Complaints with the HVAD Internal Controller Alarm Battery failures.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· Siemens Healthcare Diagnostics, Inc.

Recalled Item: EasyLink Data Management System Recalled by Siemens Healthcare Diagnostics,...

The Issue: System Limitations and Software Issues related to the following features:...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...

The Issue: Complaints with the HVAD Abnormal Power Source Switching.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· Richard-Allan Scientific Company

Recalled Item: Mucolytic Agent 1 pint/473 ml Recalled by Richard-Allan Scientific Company...

The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and...

The Issue: HeartWare has received complaints relating to damage or bent connection pins...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 29, 2015· Zimmer, Inc.

Recalled Item: Cortical Screw for M/DN Intramedullary Fixation. Metaphyseal/Diaphyseal Nail...

The Issue: The entire scope of 4.5mm Cortical Screws listed as compatible with the M/DN...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· Richard-Allan Scientific Company

Recalled Item: Lerner Laboratories Mucolexx Recalled by Richard-Allan Scientific Company...

The Issue: Richard Allan Scientific (RAS) is initiating a recall of Mucolytic agent and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac...

The Issue: Complaints with the HVAD Discolored and Cracked Driveline Outer Sheath.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2015· HeartWare Inc

Recalled Item: HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product...

The Issue: Failures of the splice repair kit if exposed to excessive force.

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

Class I — Serious Health HazardOngoing