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. 2,953 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,953 in last 12 months

Showing 1454114560 of 56,506 recalls

DrugFebruary 10, 2022· Positive Health

Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 10, 2022· Vbest Inc

Recalled Item: Salted Dried Plums Recalled by Vbest Inc Due to Firm supplied salted dried...

The Issue: Firm supplied salted dried plums (Saladitos) to two firms who are recalling...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 10, 2022· J & M Foods, Inc.

Recalled Item: Favorite Day Carrot cake soft bake cookies Net Wt 8 Recalled by J & M Foods,...

The Issue: Pecans although listed in the Ingredient Statement, was omitted from the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2022· Walmart Stores

Recalled Item: Avaphinal Maximum Male Enhancement Sexual Pills Recalled by Walmart Stores...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 9, 2022· Lannett Company, Inc.

Recalled Item: Diazepam Oral Solution (Concentrate) Recalled by Lannett Company, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2022· Concord Farms, Inc.

Recalled Item: Fresh Enoki Mushrooms 5.25oz/150 g/ 34 packages per case Recalled by Concord...

The Issue: California Department of Public Health sampled product and found it to...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2022· bioMerieux, Inc.

Recalled Item: VIDAS CMV IgM Recalled by bioMerieux, Inc. Due to Invalid calibrations (out...

The Issue: Invalid calibrations (out of range high) while using the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Maquet Cardiovascular, LLC

Recalled Item: Ultima Activator II Reusable Drive Mechanism Recalled by Maquet...

The Issue: Potential for corrosion on the pins of the Ultima Activator II Reusable...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2022· ABC Sales 1 Inc

Recalled Item: MAC DADDY RED Capsules Recalled by ABC Sales 1 Inc Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2022· Your Favorite Shop

Recalled Item: THE RED PILL Recalled by Your Favorite Shop Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 8, 2022· Celebrate Today

Recalled Item: RED MAMMOTH capsules Recalled by Celebrate Today Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund