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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16041–16060 of 47,654 recalls
Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...
The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...
The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leucovorin Calcium for Injection Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...
The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A Recalled by...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan Hypodermic Safety Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...
The Issue: There is a potential that hand control units may cause the tabletop to slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection 40mg/vial For I.V. infusion only...
The Issue: Failed Impurity/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...
The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack Infant Tubingset Pixie Flow 0 Recalled by Medtronic...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.