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. 2,654 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,654 in last 12 months

Showing 4874148760 of 56,506 recalls

DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Post Procedure Cream 1 oz. containers in the Dermamedics...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 10, 2014· Dermamedics, L.L.C.

Recalled Item: Dermamedics Calm and Correct Serum Recalled by Dermamedics, L.L.C. Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined that the products...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 10, 2014· Leica Microsystems, Inc.

Recalled Item: Liquid Mouse Monoclonal Antibody CD15 (NCL-L-CD15) Recalled by Leica...

The Issue: Product does not function as intended up to the expiry date on the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2014· Tandem Diabetes Care Inc

Recalled Item: T:slim Insulin Delivery System Insulin Infusion Pump Recalled by Tandem...

The Issue: Specific lots of insulin cartridges that are used with the T:slim Insulin...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2014· Focus Diagnostics Inc

Recalled Item: Simplexa Flu A/B & RSV Direct assay Recalled by Focus Diagnostics Inc Due to...

The Issue: Focus Diagnostics is initiating an urgent safety notice correction for...

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

Class II — Potential Health HazardOngoing
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: SEXY MONKEY Recalled by Schindele Enterprises dba Midwest Wholesale Due to...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: XZONE GOLD Recalled by Schindele Enterprises dba Midwest Wholesale Due to...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: ExtenZe 600 mg Recalled by Schindele Enterprises dba Midwest Wholesale Due...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: BOOST ULTRA Recalled by Schindele Enterprises dba Midwest Wholesale Due to...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: XZEN PLATINUM Recalled by Schindele Enterprises dba Midwest Wholesale Due to...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: MiracleZEN Platinum Recalled by Schindele Enterprises dba Midwest Wholesale...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Schindele Enterprises dba Midwest Wholesale

Recalled Item: Magic For Men Recalled by Schindele Enterprises dba Midwest Wholesale Due to...

The Issue: Marketed Without an Approved NDA/ANDA: These dietary supplements contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 9, 2014· Hospira Inc.

Recalled Item: Aminosyn 3.5% M Sulfite-Free Recalled by Hospira Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 9, 2014· Hospira Inc.

Recalled Item: Heparin Sodium 2000 USP Heparin Units per 1000 mL (2 Recalled by Hospira...

The Issue: Lack of Assurance of Sterility; potential leakage from administrative port.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 9, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products White Slides Recalled by Ortho-Clinical...

The Issue: An incorrect assay value (0.3785) was printed on the product carton for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-AB Abdominal Dressing Kit with Soft Port Recalled by...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS Soft Port (The RENASYS Recalled by Smith & Nephew...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-F Foam Dressing Kit with Soft Port REF #'s: 66800794...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-G Sterile Recalled by Smith & Nephew Inc. Due to...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2014· Smith & Nephew Inc.

Recalled Item: Smith & Nephew RENASYS-Gauze with Soft Port Kit REF #'s: 66800933 Recalled...

The Issue: Reports of wound fluid and /or blood that were not evacuated from beneath...

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

Class II — Potential Health HazardOngoing