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. 1,095 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,095 in last 12 months

Showing 25321–25340 of 56,506 recalls

DrugMarch 7, 2019· Medtech Products, Inc.

Recalled Item: Little Remedies New Baby Essentials Kit. Each kit contains 1 Recalled by...

The Issue: Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 7, 2019· GOOD KARMA FOODS INC

Recalled Item: PL Trader Joe Natural Creamer - Vanilla 12/32oz Recalled by GOOD KARMA FOODS...

The Issue: Product was recalled due to undeclared milk. The Contains statement does not...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...

The Issue: The heated tube sets were consistently leaking and detaching from the cassette.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Abbott Gmbh & Co. KG

Recalled Item: Abbott Alinity ci-series System Control Module software version 2.5.1...

The Issue: Potential performance issues in the Alinity-ci software version 2.5.1

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There were multiple issues identified in the system software which required...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica Sample Handler Prime Recalled by Siemens Healthcare Diagnostics,...

The Issue: There were multiple issues identified in the system software which required...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There were multiple issues identified in the system software which required...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· BioFire Diagnostics, LLC

Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to Potential...

The Issue: Increased risk of false positive Enterobacteriaceae and Escherichia coli...

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2019· American Health Packaging

Recalled Item: Valsartan Tablets USP 160 mg Recalled by American Health Packaging Due to...

The Issue: CGMP Deviation: Presence of NDEA (N-Nitrosodimethylamine), a carcinogen...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 6, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Docetaxel Injection USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Defective Container: complaint for seal and cap vial issues that could lead...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2019· Acclarent, Inc.

Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...

The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· Acclarent, Inc.

Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...

The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· Acclarent, Inc.

Recalled Item: TruDi NAV Suction Recalled by Acclarent, Inc. Due to The firm became aware...

The Issue: The firm became aware that three (3) lots of the NAV Suction Instruments...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· BioFire Diagnostics, LLC

Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...

The Issue: Elevated rates of false positive results for Campylobacter and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· Topcon Medical Systems, Inc.

Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...

The Issue: When a patient is selected in the patient data and another patient is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2019· PROCEPT BIOROBOTICS CORPORATION

Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...

The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2019· USA LESS Inc.

Recalled Item: LEOPARD Miracle Honey packaged in a wooden box Recalled by USA LESS Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: product tainted with undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 5, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium and Hydrochlorothiazide Tablets Recalled by AVKARE Inc....

The Issue: CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA)...

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

Class II — Potential Health HazardOngoing
Refund