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. 2,881 recalls have been distributed to California in the last 12 months.
Showing 19701–19720 of 56,506 recalls
Recalled Item: uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This Recalled by...
The Issue: 1) Service function problem may cause false marking of a bad channel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointts sistema de ellmlnact! Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personelle OTC Skin Tag Remover Recalled by OraSure Technologies, Inc. Due...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Advanced Wart Remover Kit Recalled by OraSure Technologies, Inc. Due to...
The Issue: Unit boxes not properly sealed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SINGLES Carbide US-No. FG556 Recalled by Hager & Meisinger Gmbh Due to...
The Issue: US-dates between the product package label and the bar code display.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QIAstat-Dx Respiratory SARS-CoV-2 Panel (US IVD under FDA Recalled by Qiagen...
The Issue: There is an increased rate of potential false positive results for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models FR4A-SPR-BO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model FR4A-TRL-AO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-RCV-AO US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model 1. STQ4-RCV-A0 US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Models: 1. FR4A-TRL-BO US...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StimQ Peripheral Nerve Stimulator System (PNS) Model STQ4-SPR-BO US -...
The Issue: The product contains a non-functional component not in product labeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniTom Computed tomography x-ray system Recalled by NeuroLogica Corporation...
The Issue: There are potential issues related to the operational state of the scanner,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Patch 5% Recalled by Teva Pharmaceuticals USA Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp date on the individual...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wuxi Nest Recalled by Thomas Scientific Due to The firm is replacing all...
The Issue: The firm is replacing all tubes that were manufactured and distributed prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Recalled by Siemens...
The Issue: Hardware error- Hot Plugging feature could cause an electrical malfunction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Stapes Protheses Piston 0.6mm X 4.25 mm- Partial Ossicular Recalled by...
The Issue: Mislabeled outer carton: packaged with the outer carton label stating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smart Stapes Protheses Piston 0.4mm X 5.25 mm- Partial Ossicular Recalled by...
The Issue: Mislabeled outer carton: packaged with the outer carton label stating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrocortisone butyrate Cream Recalled by Bausch Health Companies, Inc. Due...
The Issue: SUBPOTENT DRUG
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fosaprepitant for Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Labeling Error: Label Error on Declared Strength: Carton label and product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.