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. 2,940 recalls have been distributed to California in the last 12 months.
Showing 16861–16880 of 30,923 recalls
Recalled Item: Nuclear Magnetic Resonance Imaging Systems that are indicated for use...
The Issue: When using respiratory gating with Steady Mode ON in Spin Echo sequence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLOSEAL Special Applicator Tips in cartons labeled in part Recalled by...
The Issue: Baxter r recalled this device due to the use of an incorrect plastic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno Recalled by Siemens Medical Solutions USA, Inc Due to During...
The Issue: During manual LAO/RAO rotation at maximum speed or a combination of LAO/RAO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implant Direct Legacy Implant Closed-Tray Transfer-Concave Profile Recalled...
The Issue: Cap may be mislabeled with incorrect part number, although the correct part...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disinfection unit UV (432332-9020-000) for the Celldiscoverer 7 microscope...
The Issue: Under certain circumstances, the firmware makes it possible for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 DR Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 Pro Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 ES Recalled by GE Healthcare, LLC Due to When your...
The Issue: When your system was installed, the Main disconnect switch, EPO button on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...
The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima CT 540 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution EVO 3.6 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MI Digital Ready Recalled by GE Healthcare, LLC Due to DIGITAL...
The Issue: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.