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 26461–26480 of 30,923 recalls
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The NAV3i Platform Power Box supplies the electrical components with...
The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design Recalled by AMO...
The Issue: Units may be labeled with the incorrect diopter power.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic M-IV Mammography System Recalled by Hologic, Inc. Due to Selenia...
The Issue: Selenia Full Field Digital Mammography System defective relay switch, if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker NAV3i Platform is a mobile cart platform consisting Recalled by...
The Issue: The Stryker NAV3i Platform Power Boxes produced between December 9, 2013 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cooper Surgical TAMPA CATHETER 5 French 33 cm. Intended for Recalled by...
The Issue: Sterility of the device may be compromised due to unsealed pouch
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Selenia Full Field Digital Mammography System: SEL-00002 Recalled by...
The Issue: Selenia Full Field Digital Mammography System defective relay switch, if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Armstrong Grommet with wire Otological Ventilation Tube Catalog #:...
The Issue: One lot of ventilation tubes have mixed tubes with wire attached to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products FS Calibrator 1 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toshiba Infinix X-Ray Interventional System INFX-8000V/UU. An X-Ray system...
The Issue: Although the Flat Panel Detector (FPD) touch sensor is activated during use,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...
The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips...
The Issue: Potential for the Fenestrated Grasper Tip jaw to break when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS (R) Chemistry Products Calibrator Kit 17 Recalled by Ortho-Clinical...
The Issue: Calibrator values assigned for the calibrator kit lots were released using a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs Healthcare Ventilator Flexport Interface Recalled by Spacelabs...
The Issue: Spacelabs Healthcare is voluntarily recalling the Hamilton Galileo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProBeam Proton Therapy System (HGA and HFB) Product Usage:ProBeam Proton...
The Issue: Anomaly with the ProBeam System where under certain conditions, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apex Arc Hip Stem Recalled by Omnilife Science Inc. Due to Staining on hip...
The Issue: Staining on hip implant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000...
The Issue: Physio-Control has become aware of incidents where customers have attempted...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Ysio Systems Product Usage: The Ysio (New RAD-FAMILY) systems...
The Issue: Excessive usage of cleaning liquid on Siemens Ysio Systems may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Recalled...
The Issue: There is a potential fire hazard of certain Lithium-Ion batteries in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACROLYTE Premie Dispersive Electrode Recalled by ConMed Corporation Due to...
The Issue: ConMed Corporation has received complaints regarding sparking, no output and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.