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. 2,840 recalls have been distributed to Washington in the last 12 months.
Showing 3001–3020 of 51,768 recalls
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Recalled by...
The Issue: The potential for cracks forming in the breathing circuit hose.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 Whole Foods Market Small Bites Macaroni & Cheese. Net Recalled by C.H....
The Issue: Undeclared allergen (eggs) and pork
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CVS Health Concealing Acne Treatment Cream Recalled by Fruit Of The Earth,...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...
The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Ophthalmic Solution USP Recalled by FDC Limited Due to...
The Issue: Defective container: Unable to get the solution out of the bottle as the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...
The Issue: Users trying to restock a single bin location of an automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 4 Fr Single-Lumen PowerPICC Catheters Recalled by Bard Access Systems,...
The Issue: Catheters indicated for short-or-long term access to the central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...
The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...
The Issue: Incorrect software flagging may occur for the assay that may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID Recalled...
The Issue: Due to a software issue, when attempting to restock the automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...
The Issue: Nerve Monitoring System with certain software versions has potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...
The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...
The Issue: The devices are missing the laser marked depth markings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.