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. 1,118 recalls have been distributed to California in the last 12 months.
Showing 19141–19160 of 56,506 recalls
Recalled Item: Niobe ES System Recalled by Stereotaxis Inc Due to There is a potential for...
The Issue: There is a potential for fire in the inside computer cabinet.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...
The Issue: Potential malfunction in which the examination room monitor may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...
The Issue: California Department of Public Health sampled and tested Shirakiku brand...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (femur)...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails Recalled by Merete...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (humerus)...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoBridge Intramedullary Diaphysis Segment Fixation (IDSF) nails (tibia)...
The Issue: Product may be mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-i Ventilator Recalled by Getinge Group Logistics America, LLC Due to A...
The Issue: A potentially shorter than specified nebulizer connector may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Recalled...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...
The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.