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. 1,043 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,043 in last 12 months

Showing 42561–42580 of 56,506 recalls

Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· RAYSEARCH LABORATORIES AB

Recalled Item: RaySearch RayStation 2.5 Recalled by RAYSEARCH LABORATORIES AB Due to...

The Issue: RaySearch Laboratories AB became aware of an issue with the dose calculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· Covidien LP (formerly Nellcor Puritan Bennett Inc.)

Recalled Item: Shiley Neonatal Recalled by Covidien LP (formerly Nellcor Puritan Bennett...

The Issue: Reports where patients who recently switched from the current Shiley...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 8, 2015· Gyrus Acmi, Incorporated

Recalled Item: Gyrus ACMI Diego Elite Tubeset Recalled by Gyrus Acmi, Incorporated Due to...

The Issue: Potential lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
FoodMay 8, 2015· Bruce Foods Corporation

Recalled Item: Del Pasado Dice Green Chiles 100% Fire Roasted and Peeled Recalled by Bruce...

The Issue: Metal

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 8, 2015· Natural Creations Inc

Recalled Item: 250cc White Plastic Container containing 120 capsules Recalled by Natural...

The Issue: Natural Creations announces allergy alert and voluntary recall of New...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 7, 2015· Teva Pharmaceuticals USA

Recalled Item: QVAR (beclomethasone dipropionate HFA 40 mcg) Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: out of specification test...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: HDL-Cholesterol gen.3. For the quantitative determination of high-density...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Viewray Incorporated

Recalled Item: Treatment Planning and Delivery System Software version 3.6. ViewRay....

The Issue: The software was failing to determine new patient locations if imaging is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Triglycerides GPO. In vitro test for the quantitative determination of...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2)...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Ocean Water Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems Recalled...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Atrium Medical Corporation

Recalled Item: EXPRESS Dry Seal Chest Drain Recalled by Atrium Medical Corporation Due to...

The Issue: Chest drains have a missing o-ring

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2015· Roche Diagnostics Operations, Inc.

Recalled Item: Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the...

The Issue: Possible drug interference when using the Trinder reaction method on...

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

Class II — Potential Health HazardOngoing