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. 1,177 recalls have been distributed to California in the last 12 months.
Showing 14021–14040 of 30,923 recalls
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Urinalysis Control Level 2 (IVD) - Product Recalled by Randox...
The Issue: Analyte range for Leukocytes for use with the Siemens Multistix method is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HS70A Diagnostic Ultrasound System Version 2.01.00 Recalled by NeuroLogica...
The Issue: There is a potential for probes overheating when decreasing the Doppler SV...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...
The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Threaded Offset Cup Impactor - Product Usage: To assist the Recalled by...
The Issue: The threaded mechanism of the Threaded Offset Cup Impactor may be gritty and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan BioDIMENSIONAL silicone-Filled Breast Implants Recalled by Allergan...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.