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 1701–1720 of 51,768 recalls
Recalled Item: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial use Recalled by Max...
The Issue: Due to a faulty electrical connection between the speed control Dial and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...
The Issue: Limited system movements after startup .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lisdexamfetamine Dimesylate Capsules Recalled by Lannett Company Inc. Due to...
The Issue: Labeling: Label Mix-up. A bottle labeled as Lisdexamphetamine Dimesylate...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number:...
The Issue: Potential for falsely depressed patient, quality control (QC), and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to Merge Healthcare has...
The Issue: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Theophylline extended-release tablets 400mg Recalled by Glenmark...
The Issue: Failed Dissolution Specifications: Failure results (above) were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...
The Issue: Blood collection tubes were manufactured with the label applied too high on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring...
The Issue: Vital sign monitoring instrument may trigger an error message during blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...
The Issue: Software issue that results in the display of outdated information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.