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. 2,836 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,836 in last 12 months

Showing 3038130400 of 30,923 recalls

Medical DeviceMay 9, 2012· Natus Medical Incorporated

Recalled Item: The product has the Catalogue/Part number 60010. Olympic Cool-Cap System...

The Issue: The Olympic Cool-Cap's Control Module has experienced a frozen screen during...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2012· RAYSEARCH LABORATORIES AB

Recalled Item: Brand name: RayStation. Generic name: Treatment Planning System. Software...

The Issue: The firm decided to recall when an issue was found with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...

The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· JK Products & Services, Inc

Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...

The Issue: The Beauty Angel was marketed without a 510k.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Non-Invasive Monitoring Systems, Inc.

Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...

The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO General Purpose Sensor Recalled by Civco Medical Instruments Inc Due...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Civco Medical Instruments Inc

Recalled Item: CIVCO VirtuTRAX Instrument Navigator Recalled by Civco Medical Instruments...

The Issue: The general purpose electromagnetic sensor was incorrectly calibrated...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Mindray DS USA, Inc. d.b.a. Mindray North America

Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...

The Issue: Mindray has identified two software anomalies contained in the V Series...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: The Brilliance iCT and iCT SP are Computed Tomography X-Ray Recalled by...

The Issue: Philips is issuing a software update (version 3.2.4) to the Brilliance iCT...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· Non-Invasive Monitoring Systems, Inc.

Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...

The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2012· MTI Precision Products LLC.

Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...

The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Stanley Security Solutions, Inc.

Recalled Item: Tabs Professional Monitor Recalled by Stanley Security Solutions, Inc. Due...

The Issue: The monitor may fail to sound an alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 6IN Side-Fire Needle Recalled by DePuy...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 13G X 6IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: Depuy Spine Side Fire Needles 11G X 4IN Recalled by DePuy Mitek, Inc., a...

The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2012· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Scenaria CT System Software Product Usage: The Scenaria system...

The Issue: Hitachi discovered a software error in the Reconstruction Status function...

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

Class II — Potential Health HazardOngoing