Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,020 recalls have been distributed to Delaware in the last 12 months.
Showing 1601–1620 of 48,330 recalls
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: RayStation with the following product descriptions: 1. RayStation 2023B...
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: 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: 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: 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 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: 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The Issue: Software issue that results in the display of outdated information.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 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 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.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...
The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xpert SA Nasal Complete Catalog Number: GXSACOMP-10 UDI-DI code:...
The Issue: As a result of Post-Market half-time stability testing, false negative test...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...
The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.