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. 1,965 recalls have been distributed to Washington in the last 12 months.
Showing 18421–18440 of 29,208 recalls
Recalled Item: Neusoft NeuViz 128 Multi-slice CT Scanner System Product Usage: The Recalled...
The Issue: Software defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP Latex Reagent Recalled by Fisher Diagnostics Due to...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30...
The Issue: An issue was discovered with the Pacific Hemostasis Fibrinogen Degradation...
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: 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: 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: 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: 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: 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: 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 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: 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: 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.
Recalled Item: Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics...
The Issue: During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have...
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: Signa PET/MR (K163619 Recalled by GE Medical Systems, LLC Due to Possible...
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: Brivo MR355 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.