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. 2,856 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,856 in last 12 months

Showing 2272122740 of 56,506 recalls

FoodSeptember 11, 2019· Lion Foods

Recalled Item: Greenland All Natural Gourmet Crispy Fried Onions NET WT 400g Recalled by...

The Issue: Potential metal contamination

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 11, 2019· Urban Remedy

Recalled Item: Green Tea Leaf Salad 6.7 oz. Recalled by Urban Remedy Due to Potential E....

The Issue: Random sampling of spinach from vendor found Enterohemorrhagic E-Coli/Shiga...

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

Class I — Serious Health HazardOngoing
Refund
FoodSeptember 11, 2019· Urban Remedy

Recalled Item: The Benedict Brunch Bowl Recalled by Urban Remedy Due to Potential E. coli...

The Issue: Random sampling of spinach from vendor found Enterohemorrhagic E-Coli/Shiga...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Novarad Corporation

Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...

The Issue: The firm received a report of an atypical dataset being generated. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /1000g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1700-10. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a /980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1400-04. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1500-04-S. For...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Candela Corporation

Recalled Item: Canister HFC-134a / 980g Recalled by Candela Corporation Due to The canister...

The Issue: The canister neck bushing may become loose and separate from the body of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Philips North America LLC

Recalled Item: Philips HeartStart FRx AED Recalled by Philips North America LLC Due to...

The Issue: Affected devices contain a Printed Circuit Assembly (PCA) that was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Alto Development Corp

Recalled Item: A&E Medical Thorecon Plating System Kits Model No. 94-1200-08. For Recalled...

The Issue: Some Thorecon disposable tensioners supplied in different Plating System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· MEDTECH SAS

Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...

The Issue: The instrument holder may be sent on a trajectory that is not within the...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Philips North America LLC

Recalled Item: Philips HeartStart HS1 Onsite (Model M5066A) and HSI Home (Model M5068A) AED...

The Issue: Affected devices contain a Printed Circuit Assembly (PCA) that was not...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

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

Class II — Potential Health HazardOngoing