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. 2,602 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,602 in last 12 months

Showing 3686136880 of 51,768 recalls

Medical DeviceJanuary 19, 2016· Sorin Group USA, Inc.

Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...

The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 18, 2016· Sedecal S.A.

Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...

The Issue: This is related to previous 806 Notifications about uncommanded movements of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2016· Philips Respironics

Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue

The Issue: Software Issue

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...

The Issue: To inform users about the possible incorrect values for Distance...

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Amerisource Health Services

Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...

The Issue: Failed Dissolution Specifications: Unexplained low out of specification...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Bausch & Lomb, Inc.

Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...

The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2016· Perrigo Company PLC

Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...

The Issue: Labeling: label error on declared strength.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2016· Master Herbs, Inc./Li

Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...

The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· Heritage International

Recalled Item: Trader Joe's Nuts Raw Cashew Pieces NET Wt. 18 oz Recalled by Heritage...

The Issue: Heritage International USA, Inc. is recalling Trader Joe's Raw Cashew Pieces...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· NutraKey, Inc.

Recalled Item: VPro Raw Plant Protein Recalled by NutraKey, Inc. Due to Undeclared Soy

The Issue: Undeclared Soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 15, 2016· Hain Celestial Group

Recalled Item: Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17...

The Issue: Hain Celestial Seasoning is recalling Celestial Seasonings Roastaroma Herbal...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 15, 2016· CareFusion 303, Inc.

Recalled Item: Jadak Barcode Scanner Recalled by CareFusion 303, Inc. Due to Customers...

The Issue: Customers reported issues when scanning medications with the scanners. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 15, 2016· OraSure Technologies, Inc.

Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...

The Issue: OraSure Technologies, Inc. discovered the package insert included with the...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 15, 2016· The Anspach Effort, Inc.

Recalled Item: Universal Battery Charger II (UBC II) Recalled by The Anspach Effort, Inc....

The Issue: The device is reported to enter safe mode and is no longer able to charge...

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

Class II — Potential Health HazardOngoing