Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,724 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,724 in last 12 months

Showing 1812118140 of 51,768 recalls

Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: 9100c NXT system - Product Usage: Device is licensed and Recalled by GE...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Avance CS2 Anesthesia System - Product Usage: intended...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: Flow Sensor Service Part Recalled by GE Healthcare, LLC Due to Flow sensors...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· GE Healthcare, LLC

Recalled Item: GE Datex-Ohmeda Aisys CS2 Anesthesia System - Product Usage: is Recalled by...

The Issue: Flow sensors could have damaged tubes in the form of small punctures or cuts.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2020· Quidel Corporation

Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...

The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...

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

Class II — Potential Health HazardOngoing
DrugSeptember 16, 2020· Arbor Pharmaceuticals Inc.

Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
DrugSeptember 16, 2020· Perrigo Company PLC

Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...

The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...

The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2020· Boston Scientific Corporation

Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...

The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: Novaplus Monitoriing Electrode with Foam Tape and Sticky Gel - Recalled by...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 15, 2020· 3M Company - Health Care Business

Recalled Item: 3M Red Dot Monitoring Electrode with 4mm Adapter - Product Recalled by 3M...

The Issue: Corrosion could cause performance failures in the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Philips North America, LLC

Recalled Item: Philips Sterilizable Defibrillator Paddles Recalled by Philips North...

The Issue: The periodic Paddle Checks recommended in the Instructions for Use for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Philips North America, LLC

Recalled Item: Philips Sterilizable Defibrillator Paddles Recalled by Philips North...

The Issue: The periodic Paddle Checks recommended in the Instructions for Use for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 14, 2020· Becton Dickinson & Company

Recalled Item: BD Nexiva Closed IV Catheter System Dual Port (20 GA Recalled by Becton...

The Issue: Dull/blunt needles within the IV Catheter System may lead to missed...

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

Class II — Potential Health HazardOngoing