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. 2,856 recalls have been distributed to California in the last 12 months.
Showing 22861–22880 of 30,923 recalls
Recalled Item: Zimmer Periarticular Locking Plate System 3.5mm Locking Screw 58 mm Length...
The Issue: Product on the package label did not match what was inside the package. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ Oncology Information System MOSAIQ is an oncology information system...
The Issue: Incorrect drug dosage due to "Age Limit" and patient weight data item issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Lumify Diagnostic Ultrasound Recalled by Philips Ultrasound, Inc....
The Issue: Color Flow direction is displayed incorrectly in Lumify 1.0. The system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AltiVate Reverse Humeral Broach Recalled by Encore Medical, Lp Due to The...
The Issue: The trial shell mating feature on the broach is undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Oscillating Flat - TS ST Hub Recalled by Synvasive Technology Inc Due...
The Issue: Two lots of oscillating saw blades incorrectly identify the blade cutting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 10-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 2-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SYNTHECEL Dura Repair Recalled by Synthes (USA) Products LLC Due to It was...
The Issue: It was reported that the SYNTHECEL Dura Repair could adhere to various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer ClWIZARD2 5-detector Recalled by Perkinelmer Due to The content...
The Issue: The content of the second #023 barcode ID label in the Barcode ID Label...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Rod Cat. No.: SR 55100 5.5 x 100 Recalled by Innovasis, Inc Due...
The Issue: Innovasis recalled two lots of Excella II titanium rods which were packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Possible installation error of the quench lines of superconducting magnets,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Coil overheating...
The Issue: Coil overheating can occur when the device is used in Mode 2 setup. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.