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 48761–48780 of 56,506 recalls

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
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: 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
FoodJanuary 8, 2014· Washington Vegetable Co

Recalled Item: Cactus Pads (Nopal) Mexpogroup: Product of Mexico Recalled by Washington...

The Issue: Unapproved pesticides were found by the CA Department of Pesticide...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 8, 2014· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panaroma Central Station Product Usage: This device can view real time...

The Issue: Mindray has identified two issues with the Panorama Central Station. Full...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· The Anspach Effort, Inc.

Recalled Item: ANSPACH Cutting bur Recalled by The Anspach Effort, Inc. Due to Anspach...

The Issue: Anspach product code L-3SD contained product code S-3SD which is shorter in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· Veridex, LLC

Recalled Item: CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS...

The Issue: Janssen Diagnostics, LLC received complaints of camera failures on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· B. Braun Medical, Inc.

Recalled Item: SAFSITE¿ Injection Sites and IV Sets manufactured with SAFSITE¿ Injection...

The Issue: Complaints were received reporting leakage on certain lots of SAFSITE¿...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2014· AGFA Corp.

Recalled Item: IMPAX RIS QDOC 5.8 Recalled by AGFA Corp. Due to Patient name displayed...

The Issue: Patient name displayed (printed) on the Patient Report was the wrong patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Drill Template and the Saw Guide for the Ulna Osteotomy Recalled by Synthes,...

The Issue: The Drill Template and the Saw Guide for the Ulna Osteotomy System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Churchill Medical Systems, Inc.

Recalled Item: AMS-530 7 Microbore Trifurcated Extension sets Product Usage: Intravascular...

The Issue: Defective component may cause extension sets to leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2014· Synthes, Inc.

Recalled Item: Synthes Driving Cap/Threaded Both parts are intended for use in Recalled by...

The Issue: The Synthes Driving Cap/Threaded can bind in the IM Nail Radiolucent...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Roche Molecular Systems, Inc.

Recalled Item: cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Recalled by Roche...

The Issue: Numerous complaints have been filed that leaking cobas ¿ PCR media 4.3 mL...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2014· Teleflex Medical

Recalled Item: ISIS HVT Tracheal Tube Cuffed with Subglottic Secretion Suction Port...

The Issue: The tracheal tube can kink during patient use.

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

Class I — Serious Health HazardOngoing