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. 2,798 recalls have been distributed to Washington in the last 12 months.
Showing 8881–8900 of 51,768 recalls
Recalled Item: Greek Orzo Pasta Salad is a food service product Recalled by Eat Good LLC...
The Issue: Label declares orzo and feta cheese but does not declare orzo pasta (wheat)...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Caesar Pasta Salad is a food service product Recalled by Eat Good LLC Due to...
The Issue: Label declares Pasta, Parmesan cheese, Mayonnaise but does not declare...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elote Corn Salad is a food service product Recalled by Eat Good LLC Due to...
The Issue: Label declares feta cheese but does not declare Milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mandarin Noodle Salad is a food service product Recalled by Eat Good LLC Due...
The Issue: Label declares pasta but does not declare wheat.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mediterranean Salad is a food service product Recalled by Eat Good LLC Due...
The Issue: Label declares pepperoncini but does not declare sulfite and FD&C Yellow #5....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Impella RP Flex with SmartAssist intracardiac microaxial blood pump Recalled...
The Issue: A higher than expected rate of thrombus formation or deposition has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Neuro Match Head Recalled by Stryker Corporation Due to There...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Precision Neuro Match Head Recalled by Stryker Corporation Due...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is Recalled by...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion FMS Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legion FMS Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring system Recalled by Medtronic...
The Issue: Product labeling contains incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.