Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,026 recalls have been distributed to District of Columbia in the last 12 months.
Showing 14281–14300 of 47,654 recalls
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Starbucks Doubleshot Espresso Recalled by Pepsico Inc Due to An issue with...
The Issue: An issue with adequate sealing of canned coffee products potentially lead to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...
The Issue: When the user presses or releases both the APC (accept) button and the Float...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error, the software can produce an incorrect interpretation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...
The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...
The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...
The Issue: A software anomaly may occur with the clinician programmer application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS B.R.A.H.M.S. PROCALCITONIN PCT Recalled by bioMerieux, Inc. Due to...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM SARS-CoV-2 Antigen Assay (100 Test Kit) Recalled by Siemens...
The Issue: Data provided in the Emergency Use Authorization (EUA) submission was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS FSH Recalled by bioMerieux, Inc. Due to bioMerieux has been receiving...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...
The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS RUB IgG (RBG) Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...
The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS SARS-COV-2 IgM Recalled by bioMerieux, Inc. Due to bioMerieux has been...
The Issue: bioMerieux has been receiving an increasing number of complaints linked to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.