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. 2,674 recalls have been distributed to Delaware in the last 12 months.
Showing 5181–5200 of 48,330 recalls
Recalled Item: NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with...
The Issue: Potential for false negative response on the NIM Vital Nerve Monitoring System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diflorasone Diacetate Ointment Recalled by Rising Pharma Holding, Inc. Due...
The Issue: Failed Impurities/Degradation Specifications: The impurity results at 12...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion Hydrochloride Extended-release Tablets USP (XL) Once-Daily...
The Issue: Failed Dissolution Specifications; the product is dissolving faster than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ESG-410 Electrosurgical Generator- In conjunction with electrosurgical...
The Issue: Electrosurgical Generators ESG-410 does not power on upon use, may result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetaminophen Extra Strength Tablets Recalled by A-S Medication Solutions...
The Issue: Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules Recalled by Zydus...
The Issue: Failed Dissolution Specifications: Out-of-specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cepheid Recalled by Cepheid Due to Specimen collection device may leak after...
The Issue: Specimen collection device may leak after the patient sample swabs have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Moon Essentials Recalled by Little Moon Essentials LLC Due to CGMP...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Verigene Gram Positive Blood Culture (BC-GP) Nucleic Acid Test Recalled by...
The Issue: Potential for defective test cartridges which may result in false positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel Recalled by BioFire...
The Issue: If blood culture identification panel is used in conjunction with specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 38mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 42mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNITRAX Endoprosthesis Head Component - 43mm. Implantable component used in...
The Issue: Mislabeled: the size on the package label of the UNITRAX¿ Endoprosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.