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. 2,828 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,828 in last 12 months

Showing 3184131860 of 56,506 recalls

Medical DeviceJune 19, 2017· ConMed Corporation

Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...

The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· ConMed Corporation

Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...

The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· Nova Biomedical Corporation

Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...

The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2017· Leica Microsystems, Inc.

Recalled Item: Nussloch GmbH ASP6025 Tissue Processor Recalled by Leica Microsystems, Inc....

The Issue: Incorrect labeling for specified voltage for the Alarm Connectors on the...

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

Class II — Potential Health HazardOngoing
FoodJune 17, 2017· House Of Thaller Inc

Recalled Item: Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g) Recalled by...

The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 17, 2017· House Of Thaller Inc

Recalled Item: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g) Recalled by...

The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 17, 2017· House Of Thaller Inc

Recalled Item: LANTANA White Bean HUMMUS NET WT. 10 oz (283g) Recalled by House Of Thaller...

The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 16, 2017· Time-Cap Laboratories, Inc.

Recalled Item: Ibuprofen Tablets Recalled by Time-Cap Laboratories, Inc. Due to Presence of...

The Issue: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2017· Alvogen, Inc

Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2017· Alvogen, Inc

Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 16, 2017· Alvogen, Inc

Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 16, 2017· Threshold Enterprises Ltd

Recalled Item: Planetary Herbals Ginseng Classic Recalled by Threshold Enterprises Ltd Due...

The Issue: Product was inadvertently released prior to release of all QC testing....

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 16, 2017· Rikki USA, Inc.

Recalled Item: Masas Gourmet Curry Coconut Sauce Recalled by Rikki USA, Inc. Due to Curry...

The Issue: Curry Coconut Sauce is recalled because the Ingredients Statement declared...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 16, 2017· Rikki USA, Inc.

Recalled Item: Masas Gourmet Pulled Pork BBQ Sauce Recalled by Rikki USA, Inc. Due to...

The Issue: Pulled Pork BBQ Sauce is recalled because the Ingredients Statement declared...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 16, 2017· Unified Seafood Company., Inc.

Recalled Item: Pacific Wave Frozen Tuna Loins Recalled by Unified Seafood Company., Inc....

The Issue: Direct customer tested tuna loins and had a positive result for Hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 16, 2017· Rikki USA, Inc.

Recalled Item: Masas Gourmet Sweet and Sour Sauce Recalled by Rikki USA, Inc. Due to...

The Issue: Sweet and Sour Sauce is recalled due to undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 16, 2017· Keystone Dental Inc

Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...

The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...

The Issue: The device failed to pump due to an electrical test failure code #58 (power...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100i Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp -...

The Issue: The device failed to pump due to an electrical test failure code #58 (power...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2017· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...

The Issue: The device failed to pump due to an electrical test failure code #58 (power...

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

Class I — Serious Health HazardOngoing