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 3618136200 of 51,768 recalls

Medical DeviceMarch 31, 2016· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Trucount Absolute Counting Tubes: Model number: 340334 IVD Recalled by...

The Issue: One lot of lot of BD Trucount tubes may contain tubes from another lot....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Shimadzu Medical Systems

Recalled Item: X-Ray Diagnostic Table Recalled by Shimadzu Medical Systems Due to Report of...

The Issue: Report of unintentional movement of table to reverse tilting.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2016· Biocare Medical, LLC

Recalled Item: Mach 4 Mouse Probe vial within the Mach 4 Universal HRP-Polymer Kit Recalled...

The Issue: Biocare Medical has identified a single lot (082715) of its Mach 4 HRP...

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

Class III — Low RiskOngoing
DrugMarch 30, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ondansetron Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications; 12 month stability time point

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur CP Immunoassay System Recalled by Siemens Healthcare...

The Issue: The firm identified an issue in sample processing when using EZee-Nest...

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

Class III — Low RiskOngoing
Medical DeviceMarch 30, 2016· Teleflex Medical

Recalled Item: Pleur-evac Chest Drainage System Recalled by Teleflex Medical Due to The...

The Issue: The label on the Tyvek bag is missing. This is used by customers to identify...

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

Class II — Potential Health HazardOngoing
FoodMarch 29, 2016· Lee Seed Co Inc

Recalled Item: Yogurt Super Soynuts packaged in 16 oz. plastic bags and Recalled by Lee...

The Issue: Product contains undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Eye Station Import Utility (ESIU) when used with Merge Recalled by...

The Issue: Eye Station images were not importing properly and were imported under...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Hemo software. Merge Hemo monitors Recalled by Merge Healthcare, Inc....

The Issue: There is a potential connection issue when powering up the Merge Hemo Record...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Product Usage: Merge Cardio is a system Recalled by...

The Issue: If a reader selects Multi-study review prior to the original study...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...

The Issue: If images are sent without an order in the system, they will be matched with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...

The Issue: Cut lines on the image may present horizontally rather than vertically.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Merge Healthcare, Inc.

Recalled Item: Merge PACS software. Product Usage: Merge PACS (Picture Archiving...

The Issue: The software did not show unviewed images when the last view was skipped....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Stryker Endoscopy

Recalled Item: PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator...

The Issue: When operating the device in high flow mode (40L/min, 15 mmHg) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Becton Dickinson & Co.

Recalled Item: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) Recalled by Becton...

The Issue: Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Boston Scientific Corporation

Recalled Item: Boston Scientific Recalled by Boston Scientific Corporation Due to Boston...

The Issue: Boston Scientific is voluntarily implementing a Medical Device Recall of one...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2016· Philips Ultrasound, Inc.

Recalled Item: EPIQ DIAGNOSTIC ULTRASOUND SYSTEM Recalled by Philips Ultrasound, Inc. Due...

The Issue: The fasteners securing the control panel assembly to the base of the Philips...

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

Class II — Potential Health HazardOngoing
DrugMarch 25, 2016· B. Braun Medical Inc

Recalled Item: 5% Dextrose Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Non-Sterility: fungal contamination due to leaking containers.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 25, 2016· Bryant Ranch Prepack Inc.

Recalled Item: Venlafaxine 75 mg Tablet Recalled by Bryant Ranch Prepack Inc. Due to...

The Issue: Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2016· Becton Dickinson & Company

Recalled Item: Henry Schein Single Use Syringe Luer-Lock Recalled by Becton Dickinson &...

The Issue: BD 10 mL Syringe Luer-Lok Tip with BD PrecisionGlide Needle 21G x 1 (0.8 mm...

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

Class II — Potential Health HazardOngoing