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. 1,013 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,013 in last 12 months

Showing 48401–48420 of 56,506 recalls

Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Buprenorphine Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Oxycodone Test Card Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Dengue NS1 Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Salmonella typhi/paratyphi Antigen Test Recalled by LumiQuick Diagnostics...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Rickettsia IgG/IgM Test Card LumiQuick Recalled by LumiQuick Diagnostics...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Cardiac Panel Test Card (Whole Blood) Recalled by LumiQuick Diagnostics Inc....

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: EDDP Strip Recalled by LumiQuick Diagnostics Inc. Due to Products shipped to...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: H. Pylori Antigen Test Card LumiQuick Recalled by LumiQuick Diagnostics Inc....

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Alcohol Test Recalled by LumiQuick Diagnostics Inc. Due to Products shipped...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: PCP Test (Strip) Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2014· LumiQuick Diagnostics Inc.

Recalled Item: Methadone Test Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...

The Issue: Products shipped to US locations that do not have approved applications for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Malleable Dual-stage Venous Return Cannulae Recalled by Terumo...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Biocardia, Inc.

Recalled Item: Morph AccessPro Steerable Introducer Recalled by Biocardia, Inc. Due to Firm...

The Issue: Firm discovered the potential for particulates in the inner lumen of Morph...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 3, 2014· Terumo Cardiovascular Systems Corporation

Recalled Item: Sarns Dual-stage Venous Return Cannulae Recalled by Terumo Cardiovascular...

The Issue: During in-process inspection, Terumo Cardiovascular Systems (Terumo CVS)...

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

Class II — Potential Health HazardOngoing