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. 2,469 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,469 in last 12 months

Showing 4448144500 of 51,768 recalls

Medical DeviceApril 1, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray...

The Issue: Siemens Radiation Oncology became aware that customers may be using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...

The Issue: Table may lose calibration during patient treatment, which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Ortho Development Corporation

Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...

The Issue: A femoral component containing pegs was found in a box for the pegless version.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Zimmer, Inc.

Recalled Item: TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to...

The Issue: The shell was missing the locking ring.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2014· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Alligator Retrieval Device (ARD). Used in the peripheral and...

The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 1, 2014· Micro Therapeutics Inc, Dba Ev3 Neurovascular

Recalled Item: Pipeline Embolization Device (PED). Used endovascular treatment of adults...

The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 31, 2014· Vidacare Corporation

Recalled Item: EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to...

The Issue: The voluntary recall is due to the needle set not meeting its specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 31, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 Recalled...

The Issue: A component on the HeartStart XL+ Therapy Board could malfunction...

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

Class II — Potential Health HazardOngoing
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: AFRICAN BLACK ANT Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Black Ant Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Xzone 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZEN PLATINUM Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZONE GOLD Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: XZEN GOLD Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: Xzen 1200 Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA: Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2014· Nova Products, Inc.

Recalled Item: MOJO RISEN Recalled by Nova Products, Inc. Due to Undeclared Amounts

The Issue: Marketed Without an Approved NDA/ANDA; Nova Products, Inc. of Aston,...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2014· Swanson Health Products, Inc

Recalled Item: Swanson Full Spectrum Cilantro (Coriander) Herbal Supplement Recalled by...

The Issue: The contract manufacturer has notified Swanson Health Products that Swanson...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 28, 2014· keen-wah LLC

Recalled Item: i heart keenwah Chocolate Sea Salt All Natural Quinoa Clusters. Recalled by...

The Issue: An anti-stick spray containing soy lecithin was used during the manufacture...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2014· keen-wah LLC

Recalled Item: i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters. Recalled by...

The Issue: An anti-stick spray containing soy lecithin was used during the manufacture...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 28, 2014· keen-wah LLC

Recalled Item: i heart keenwah Cranberry Cashew All Natural Quinoa Clusters. Recalled by...

The Issue: An anti-stick spray containing soy lecithin was used during the manufacture...

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

Class II — Potential Health HazardOngoing
Refund