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. 2,820 recalls have been distributed to Washington in the last 12 months.
Showing 5021–5040 of 51,768 recalls
Recalled Item: Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Recalled by...
The Issue: Reports have been received regarding open seals on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiomarC EX Fiducial Marker System Recalled by Carbon Medical Technologies,...
The Issue: This recall has been initiated due to a failure to provide an MRI Insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (50 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test - REF)-In vitro diagnostic Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur CA 19-9 (250 Test)-In vitro diagnostic use in Recalled by...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM CA 19-9 (250 Test)- In vitro diagnostic use Recalled by Siemens...
The Issue: Positive bias for some samples around the CA 19-9 upper limit of normal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.