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. 2,612 recalls have been distributed to Washington in the last 12 months.
Showing 30741–30760 of 51,768 recalls
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot TraumaPad Recalled by Z-Medica, LLC Due to Packaging breach may...
The Issue: Packaging breach may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV High-Density Mapping Catheter. Recalled by Biosense Webster,...
The Issue: Contraindication language updated in the Instructions For Use (IFU) to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Topical Powder Recalled by X-Gen Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Substance: potential presence of plastic particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Presence of an impurity peak...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02...
The Issue: Contraceptive Tablets Out of Sequence- First 4 pills of the packet are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ventolin HFA (albuterol sulfate) Inhalation Recalled by GlaxoSmithKline, LLC...
The Issue: Defective Delivery System: Elevated number of units with out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Beckman Coulter Synchron AQUA CAL Level 1 Recalled by Beckman Coulter Inc...
The Issue: The firm identified a negative shift of 5mmol/L for sodium recovery in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD¿ High Volume Administration Set with FlowStop Recalled by Smiths...
The Issue: One lot of CADD¿ High Volume Administration sets, part number 21-7381-24,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06...
The Issue: Potential for electric shock in the case of a failure to install the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MesaLabs Conductivity Standard Solution Recalled by Mesa Laboratories, Inc....
The Issue: Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Recalled by...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code:...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product...
The Issue: Combo Screw Driver (Product Code 288211) tip has the increased potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Creator Recalled by GE Medical Systems, LLC Due to Possible incorrect...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Flashback Needle 7cm x 18G AMC/4 Recalled by Argon Medical Devices,...
The Issue: Argon Medical has received a complaint from one of their distributors of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima MR750 3.0T Product Usage: The Optima MR450 1.5T system Recalled by GE...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MR750 3.0T Product Usage: Intended use: The Discovery MR750...
The Issue: Possible incorrect wiring of the Uninterruptable Power Supply, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.