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.
Showing 30181–30200 of 30,923 recalls
Recalled Item: AngioDynamics Angiographic catheter --- Soft-Vu (JB-1) Non-braided. ---...
The Issue: AngioDynamics is recalling one lot of Soft-Vu Angiographic catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Octane-C Cervical Recalled by Exactech, Inc. Due to Exactech, Inc. initiated...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Fixed Angle Replicator Plate Intended for Primary and Reverse...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Reverse Glenosphere Locking Screw Intended for Primary and Reverse...
The Issue: Exactech, Inc. initiated a recall of Equinoxe Replicator Plates, Equinoxe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 2.7mm Drilling Guide is a reusable instrument used in Recalled by...
The Issue: Integra' s quality system noted an adverse trend in complaints for breakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Xcelera Connect Recalled by Philips Healthcare Inc. Due to Xcelera...
The Issue: Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Single Site ADHESION BARRIER Re-order Number: 6641-01 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: seprafilm¿ Procedure Pack ADHESION BARRIER Re-order Number: 5086-02 Product...
The Issue: Sterility of product may be compromised due to packaging defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...
The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX iD HMOD 2030 Diffusion Membrane Oxygenator Recalled by Maquet...
The Issue: It has come to firm's attention that, in some rare cases, the blood outlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has become...
The Issue: GE Healthcare has become aware through complaints of a potential safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hudson RCI Concha Therm Neptune Humidifier Recalled by Teleflex Medical Due...
The Issue: Speaker Failure. If the speaker fails and an event occurs which would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-1 System Battery --- Made in U.S.A. for Carestream Health...
The Issue: Carestream DRX-1 System batteries manufactured before June 2012 due to two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fuze Manual Tilt Wheelchair. Fuze T50 Recalled by Pdg Product Design Group...
The Issue: The hex bolt head might shear and cause the axle plate to detach from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Distraction Screws of 3 different sizes: 12mm Recalled by Tedan...
The Issue: This letter is to notify you that several of our sterile screw products are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Procedural Trays: Merit's Custom Total Hip Pack Recalled by Merit...
The Issue: Custom Procedural trays contain Stryker Hytrel Togas which are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuViz 16 Multi-Slice CT Scanner System is a computed Tomography X-ray...
The Issue: One of the four screws that secure the Oil-accumulator to the X-Ray Tube...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune Bronze Rover Recalled by Stryker Instruments Div. of Stryker...
The Issue: Stryker has received two reports of serious injury as a result of tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a Image Flip Issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.