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 25001–25020 of 30,923 recalls
Recalled Item: Juno DFR X-ray system Recalled by Villa Radiology Systems LLC Due to The...
The Issue: The system does not provide the appropriate audible signal, permanent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific Creatinine Reagent Catalog number C7539-150 in vitro...
The Issue: Creatinine kit C7539-150 contains Creatinine reagent R1 that is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal...
The Issue: Teleflex Medical has issued an advisory notification for the RUSCH Curved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MUM-1 (Multiple myeloma oncogene-1) Recalled by Biocare Medical Llc Due to...
The Issue: Three lots of MUM-1 may not meet their labeled shelf life, as a drop in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autopen Classic Automatic insulin delivery pen Recalled by Owen Mumford USA,...
The Issue: The dials in the Autopens are not working - the dial does not stay dialed,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE....
The Issue: The IFU provided in the affected units of the MENTOR MemoryGel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TASP) Tibial Articular Surface Provisional Shim Recalled by Zimmer,...
The Issue: Potential for delay in surgery and/or ball bearings to be left in the wound....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis-8 Peripheral Infusion System. Models CVT808015 Recalled by...
The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01 Recalled...
The Issue: A manufacturing error resulted in the risk of incorrect proximal and distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 16cm Minimally Invasive Attachment. For use with Motor Systems for Recalled...
The Issue: Customer complaint indicating the color bands on the MIA16-G1 were not correct.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The I-Cart is used to store Recalled by Richard Wolf Medical Instruments...
The Issue: The transformers installed on carts used for Richard Wolf medical video...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...
The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX analyzer Recalled by Radiometer America Inc Due to The ABL90...
The Issue: The ABL90 analyzer does not always use the most recent calibration data to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...
The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osteobond Bone Cement Bone cement monomer is kitted with bone Recalled by...
The Issue: Samples of product from Supplier lot 14D0809 and 14D0808 showed little...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Airo Mobile Intraoperative CT I Airo Recalled by Mobius Imaging, LLC Due to...
The Issue: There is a risk that during the transfer of an image and navigation data to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...
The Issue: Invacare identified that the rail mounting bracket on the G29 full length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verasense Knee System Recalled by Orthosensor, Inc. Due to Presence of one...
The Issue: Presence of one inoperable (dead) sensor pad.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.