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. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2656126580 of 30,923 recalls

Medical DeviceApril 22, 2014· Biomet, Inc.

Recalled Item: ExploR 7x26mm Modular Radial Stem Recalled by Biomet, Inc. Due to This lot...

The Issue: This lot of the ExploR Modular Radial Stem may be missing the wedge ramp...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Hamilton Medical, Inc.

Recalled Item: HAMILTON-G5 Ventilator with software versions between V2.00 and V2.31....

The Issue: Ventilation and alarms of a HAMILTON-G5 ventilator can be suppressed...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 22, 2014· Meridian Bioscience Inc

Recalled Item: illumipro-10 Incubator/Reader Recalled by Meridian Bioscience Inc Due to...

The Issue: Illumipro-10 instruments may have Block B chambers operating at an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Synthes, Inc.

Recalled Item: Synthes Matrix Mandible Short Cut Plate Cutter Synthes Matrix Mandible...

The Issue: It was discovered internally that the face of the Synthes Matrix Mandible...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2014· Smiths Medical ASD, Inc.

Recalled Item: SW-2008 Snuggle Warm Sterile Cardiac Connective Warming Blanket Recalled by...

The Issue: The hose could separate from the blanket.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2014· Bausch & Lomb Inc- Greenville Solutions Plant

Recalled Item: Bausch & Lomb Recalled by Bausch & Lomb Inc- Greenville Solutions Plant Due...

The Issue: Out of specification results for one of the two disinfectants.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Leica Microsystems, Inc.

Recalled Item: Thyroglobulin (1D4) is a mouse anti-human monoclonal antibody produced as...

The Issue: Bond Ready to Use Primary Antibody Thyroglobulin does not function as...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 18, 2014· Med-Mizer, Inc.

Recalled Item: RetractaBed Recalled by Med-Mizer, Inc. Due to All configurations of the SS...

The Issue: All configurations of the SS Retractabed, Clinical Contour, made prior to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Elekta, Inc.

Recalled Item: HexaPOD evo RT Couchtop. To support and aid in positioning Recalled by...

The Issue: If screws are not properly tightened with a torque wrench they may become...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Teleflex Medical

Recalled Item: Hudson RCI Adult Universal Ventilator Circuit Recalled by Teleflex Medical...

The Issue: Product is being recalled due to complaints that the inspiratory and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Gen-Probe Inc

Recalled Item: APTIMA Urine Collection Kit Recalled by Gen-Probe Inc Due to Incorrect...

The Issue: Incorrect labeling was used on each pouch of the affected lots of APTIMA...

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

Class III — Low RiskOngoing
Medical DeviceApril 17, 2014· Nanosphere, Inc.

Recalled Item: Verigene Gram-Negative Blood Culture Nucleic Acid Test (BC-GN) Recalled by...

The Issue: Nanosphere has determined that a portion of BC-GN Test Cartridge Lot number...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2014· Mckesson Medical Immaging

Recalled Item: McKesson Radiology-PACS. McKesson Radiology is a medical image and...

The Issue: High priority alert icon was not displayed in the Study List when there are...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio2 PT/INR Professional Test Strips Recalled by Alere San Diego,...

The Issue: Test Strips may report an inaccurately low INR result. Several patients had...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 16, 2014· Baxter Corporation Englewood

Recalled Item: RAPIDFILL Syringe Strip Recalled by Baxter Corporation Englewood Due to...

The Issue: Possible breach in sterile barrier for inner and outer bags of the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Maquet Medical Systems USA

Recalled Item: Maquet PowerLED 700. Product Usage Recalled by Maquet Medical Systems USA...

The Issue: Maquet has identified an issue with the Maquet PowerLED 700 (certain serial...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· HeartWare Inc

Recalled Item: HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) -...

The Issue: Patients and caregivers are instructed that if a battery does not provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2014· Sakura Finetek USA Inc

Recalled Item: Tissue-Tek PARAFORM PROC/EMB/MEDIUM Recalled by Sakura Finetek USA Inc Due...

The Issue: This Lot has variations in melting temperature.

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

Class II — Potential Health HazardOngoing