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. 2,851 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,851 in last 12 months

Showing 2418124200 of 56,506 recalls

DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate Recalled by Geritrex,...

The Issue: cGMP Deviations: Products may have microbial contamination.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2019· Geritrex, LLC

Recalled Item: Gericare Geri-Tussin DM Recalled by Geritrex, LLC Due to cGMP Deviations:...

The Issue: cGMP Deviations: Products may have microbial contamination.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...

The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Paltop Advanced Dental Solutions Ltd

Recalled Item: Paltop Advanced Plus Dental Implant Dia 6.0mm L10mm Catalog Number:...

The Issue: Surface micro/nano topography on some of the implants contained within this...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Medline Industries, Inc.

Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...

The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Boston Scientific Neuromodulation Corporation

Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...

The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Ortho Development Corporation

Recalled Item: Tibial Tray Nonporous A Size 2 Recalled by Ortho Development Corporation Due...

The Issue: The locking mechanism of the tibial tray exhibited a manufacturing defect in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2019· Ortho Development Corporation

Recalled Item: Tibial Tray Nonporous A Size 4 Recalled by Ortho Development Corporation Due...

The Issue: The locking mechanism of the tibial tray exhibited a manufacturing defect in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodMay 30, 2019· Stonyfield Farm

Recalled Item: Strawberry Banana Smoothie Recalled by Stonyfield Farm Due to Mislabeling

The Issue: Strawberry Banana Smoothie Drink outside plastic wrap is mislabeled with...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 29, 2019· Siemens Healthcare Diagnostics Inc

Recalled Item: Stratus CS Acute Care cTNI TestPak Recalled by Siemens Healthcare...

The Issue: Potential for increased rate of false positive results and/or increased rate...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Liberty Cycler Cassettes (a disposable cassette that is intended to Recalled...

The Issue: Additional Instructions: step-by step handling and inserting the cassette...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· AtriCure, Inc.

Recalled Item: EPi-Sense Guided Coagulation System with Visitrax Recalled by AtriCure, Inc....

The Issue: The sterile package seal for the Epi-Sense Guided Coagulation System may be...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2019· Pega Medical Inc.

Recalled Item: SLIM Handle - catalogue #: SLM-HND100 a component of Simple Recalled by Pega...

The Issue: Handle could jam with the Driver due to the detachment of an internal...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Bio-Detek, Inc.

Recalled Item: ZOLL Pro-padz Liquid Gel Radiolucent Recalled by Bio-Detek, Inc. Due to Some...

The Issue: Some of the electrodes may have been assembled incorrectly, preventing...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568812910 Model:...

The Issue: Potential that the coating of the light head forks on the VOLISTA Surgical...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing