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. 1,777 recalls have been distributed to Washington in the last 12 months.
Showing 44481–44500 of 51,768 recalls
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.
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.
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.
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.
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.
Recalled Item: Just Great Stuff Chocolate Dream Greens Recalled by Betty Lou's, Inc. Due to...
The Issue: Undeclared milk which was a contaminant of the dark chocolate ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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.
Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...
The Issue: Urgent Device Correction notifications are being sent to USA distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...
The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: i heart keenwah Almond All Natural Quinoa Clusters. Recalled by keen-wah LLC...
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.