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. 3,026 recalls have been distributed to California in the last 12 months.
Showing 7121–7140 of 56,506 recalls
Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer is a discrete Recalled...
The Issue: The reason for the recall is the pneumatic tubing used in the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix Yeast ID Panel is a self-inoculating (when used Recalled by...
The Issue: Esculin, a substrate used in other panels and normally in A16 well, was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix NMIC-306 Panel is a self-inoculating (when used with Recalled by...
The Issue: Products were found to have confirmed drug cross contamination prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mariner RDX MIS Polyaxial Head Recalled by SEASPINE ORTHOPEDICS CORPORATION...
The Issue: Screw heads, of pedicle screw systems, have partial thread within the screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Structural Balloon Trocar Recalled by Covidien, LP Due...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Auto Suture" Blunt Tip Trocar Recalled by Covidien, LP Due to The...
The Issue: The potential for trocar seal disengagement when using mesh products...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareEvent Event Management System Recalled by Philips North America Due to...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX (PIC iX) Recalled by Philips North America Due...
The Issue: It was found that the Care Assist mobile application (version 4.1.1 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roland Tahini Recalled by Roland Foods, LLC. Due to Potential Salmonella...
The Issue: Product may be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TRIDENTII PSL CLUSTER58F-Indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER48D- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER66H- Indicated for use in primary and revision...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII HEMI CLUSTER48D-indicated for use in primary and revision patients...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER52E- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIDENTII PSL CLUSTER64H- Indicated for use in primary and revision Recalled...
The Issue: The acetabular shell may have excessive deburring, resulting in a smooth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.