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. 2,799 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,799 in last 12 months

Showing 3688136900 of 56,506 recalls

Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Procotyl (Rim- Lock) Liners: Recalled by MicroPort Orthopedics Inc. Due to...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
Medical DeviceJune 21, 2016· MicroPort Orthopedics Inc.

Recalled Item: Conserve Cups: Recalled by MicroPort Orthopedics Inc. Due to Revision rate...

The Issue: Revision rate trends from within the MicroPort Orthopedics Inc. database...

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

Class III — Low RiskOngoing
FoodJune 20, 2016· Meduri Farms Inc

Recalled Item: Meduri Farms Dried Blueberries/Sugar Infused Recalled by Meduri Farms Inc...

The Issue: Meduri Farms Dried Blueberries/Sugar Infused product is recalled due to a...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 20, 2016· Greenland Trading Corp

Recalled Item: Al Rasheed Sardine Item #4017 Label not available - NYSDAM sampling....

The Issue: Greenland Trading Corporation is recalling Al Rasheed Sardines due to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 20, 2016· Medtronic Navigation

Recalled Item: PoleStar system (N20 / N30) Warning Lamps Control Box Recalled by Medtronic...

The Issue: Medtronic Navigation is recalling certain components of the PoleStar system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to It is...

The Issue: It is possible that that the selected Plan-of-the Day could be accidently...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ Chemistry (Syva Onboard) Theophylline_2 (THEO_2) Reagent is for in...

The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Syva¿ EMIT¿ 2000 Theophylline - Catalog # 4P019UL /SMN#10445324 is Recalled...

The Issue: Siemens Healthcare Diagnostics has confirmed the Syva¿ EMIT¿ 2000...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2016· Integra LifeSciences Corp.

Recalled Item: Achillon Minimally Invasive Device for Achilles Tendon Rupture Treatment The...

The Issue: Data from internal studies suggests there may be a potential that the...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2016· Teva North America

Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL) Recalled by Teva North...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only Recalled by Teva North America Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 17, 2016· Teva North America

Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 17, 2016· Sustainable Community Development LLC dba SCD Probiotics

Recalled Item: Xtra Immunity Brown Rice Antioxidant Probiotic Extract Recalled by...

The Issue: The product is a dietary supplement with drug claims, making the product...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 17, 2016· Annona Company, LLC

Recalled Item: Earnest Eats Chewy Granola Dark Chocolate Almond .2 Recalled by Annona...

The Issue: Potential Listeria monocytogenes contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 16, 2016· Green Cuisine, Inc.

Recalled Item: Pesto Pasta Salad with Arugula Recalled by Green Cuisine, Inc. Due to...

The Issue: Green Cuisine is recalling Pesto Pasta Salad with Arugula because it may be...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX Triple Quad 4500MD LC/MS/MS System. Mass Spectrometer for Recalled...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 6.0mm Round Fluted Bur Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments initiated a voluntary recall of specific lots of Round...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 5.0mm Round Fluted Bur Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker Instruments initiated a voluntary recall of specific lots of Round...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2016· Ab Sciex

Recalled Item: AB SCIEX QTRAP¿ 4500MD LC/MS/MS System Mass Spectrometer for In-Vitro...

The Issue: MultiQuant MD software where under certain conditions a user can be...

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

Class II — Potential Health HazardOngoing