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. 2,819 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,819 in last 12 months

Showing 3456134580 of 56,506 recalls

DrugJanuary 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2017· The Harvard Drug Group

Recalled Item: Fluconazole Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 5, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Alfuzosin Hydrochloride Extended-release Tablets Recalled by Sun...

The Issue: Presence of Foreign Substance: consumer complaint for foreign matter...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 5, 2017· Haag-Streit USA Inc

Recalled Item: EyeSuite i.8.2.1.0 Software for ophthalmic use including selection of Intra...

The Issue: There is a possibility for data to be stored under the wrong patient on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2017· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...

The Issue: The company received a customer complaint for the inability to calibrate...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: IMMULITE/ IMMULITE 1000 Progesterone Recalled by Siemens Healthcare...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Dimension Vista LOCI Progesterone Recalled by Siemens Healthcare...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Progesterone Recalled by Siemens Healthcare Diagnostics, Inc...

The Issue: DHEA-S causes falsely elevated progesterone results.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Zimmer Biomet, Inc.

Recalled Item: Vanguard Total Knee System Vanguard Open Box Femoral Components Item...

The Issue: packaging of some femoral components was incorrectly labeled as either...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Baxter Healthcare Corporation

Recalled Item: Maintenance Kit PH2 Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Baxter Healthcare Corporation

Recalled Item: Maintenance Kit PH1 Recalled by Baxter Healthcare Corporation Due to Baxter...

The Issue: Baxter Healthcare Corporation is issuing a voluntary product recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX2 Endovascular AAA System Item No. Item Description F00820-01...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2017· Endologix

Recalled Item: AFX Endovascular AAA System Item Number Item Description F0070305 A2525/C75...

The Issue: Endologix updated information on the rates of Type III endoleaks and...

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

Class II — Potential Health HazardOngoing
FoodJanuary 3, 2017· Del Dee Foods Inc.

Recalled Item: Hemp & Grain Co. Recalled by Del Dee Foods Inc. Due to Potential Salmonella...

The Issue: Del Dee Foods, Inc.withdrew Lot# PP33116-0-D after receiving a report of...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2017· Bakers Of Paris, Inc.

Recalled Item: Almond Croissant:: sold in self serve cases and 4 pack Recalled by Bakers Of...

The Issue: Labeling for Croissants sold in Northern CA fails to declare egg in the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2017· Bakers Of Paris, Inc.

Recalled Item: Assorted Croissant:: sold in 4 pack clamshell package. Ingredients: Plain...

The Issue: Labeling for Croissants sold in Northern CA fails to declare egg in the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2017· Bakers Of Paris, Inc.

Recalled Item: Chocolate Croissant:: sold in self serve cases and 4 pack Recalled by Bakers...

The Issue: Labeling for Croissants sold in Northern CA fails to declare egg in the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2017· Bakers Of Paris, Inc.

Recalled Item: Croissant:: sold in self serve cases and 4 pack clamshell Recalled by Bakers...

The Issue: Labeling for Croissants sold in Northern CA fails to declare egg in the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJanuary 3, 2017· Stryker Leibinger GmbH & Co. KG

Recalled Item: 9805 Orbital Volume Sizer Set with Tray (Non-sterile) 9951 Design Recalled...

The Issue: An incorrect sterility status on the label, non-sterile products labeled as...

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

Class II — Potential Health HazardOngoing