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 2752127540 of 30,923 recalls

Medical DeviceOctober 18, 2013· Intra Pump Infusion Systems

Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...

The Issue: Product has the potential to have a clear debris on the tip of the needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Baxter Healthcare Corp

Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...

The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Del Mar Reynolds Medical, Ltd.

Recalled Item: CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation...

The Issue: Spacelabs Healthcare Ltd. of United Kingdom recalls , and Service Kits, Part...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal" Reverse Shoulder System Recalled by Zimmer, Inc. Due to As...

The Issue: As a result of complaints for disassociation of the TM Reverse Glenosphere...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Spacelabs Healthcare, Llc

Recalled Item: Spacelabs Healthcare qube Compact Patient Monitor Recalled by Spacelabs...

The Issue: Spacelabs Healthcare qube Compact Patient Monitor, Model 91390, may fail to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Philips Medical Systems North America Inc.

Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Medical Systems North America...

The Issue: A problem has been detected with Philips Model EPIQ 7 Ultrasound System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· GlaxoSmithKline, LLC.

Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Microgenics Corp

Recalled Item: Thermo Fisher Scientific/Microgenics brand CEDIA Tobramycin II Assay...

The Issue: Microgenics Corp., part of Thermo Fisher Scientific, is recalling CEDIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...

The Issue: Lens was manufactured with incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Cutera, Inc.

Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....

The Issue: Cutera received two adverse events associated with the edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Nanosphere, Inc.

Recalled Item: Nanosphere Verigene Each CDF test consists of a Verigene CDF Recalled by...

The Issue: Nanosphere has received report of an increased rate of "No Call - INT CTL 2"...

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

Class III — Low RiskOngoing
Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Radiometer America Inc

Recalled Item: ABL90 FLEX Analyzer Radiometer Medical ApS Recalled by Radiometer America...

The Issue: RADIOMETER become aware that if the ABL90 FLEX is tilted, this may...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Healthcare Informatics, Inc.

Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...

The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...

The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...

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

Class II — Potential Health HazardOngoing