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. 2,547 recalls have been distributed to District of Columbia in the last 12 months.
Showing 18141–18160 of 47,654 recalls
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Some bottles may contain mixed strengths of the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 60 Recalled by Acella Pharmaceuticals, LLC Due to Superpotent Drug.
The Issue: Superpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Saccharate Recalled by Teva Pharmaceuticals USA Due to...
The Issue: Some bottles may contain mixed strengths of the product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as Recalled...
The Issue: Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to The Substrate...
The Issue: The Substrate Monitoring System in the AIA-900 Analyzer did not detect an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VistaSolution Recalled by Vitalconnect Inc. Due to A healthcare provider...
The Issue: A healthcare provider (HCP) noticed a patient had a lowered historic SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Software Versions 3.3.3 and below...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - Software Versions 3.3.3 and Recalled by...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Software Versions 3.5.1 and below Recalled...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Software Versions 3.3.3 and below Product...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System - Product Code: 6802914 Unique Recalled...
The Issue: Modifications to MicroWell Qualitative Assay Parameters Not Retained- may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica ARveo and M530 OH6 microscope systems. Recalled by Leica Microsystems,...
The Issue: Possible unintended interruption of surgical procedures due to equipment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilretta (triamcinolone acetonide extended-release injectable suspension)...
The Issue: Temperature Abuse: Product was stored at room temperature longer than 6...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Hyclate Tablets Recalled by American Health Packaging Due to...
The Issue: Failed dissolution specification - dissolution results of 59% (spec. NLT...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LidoPro (lidocaine 4% Recalled by Wuhan Bingbing Pharmaceutical Co., Ltd....
The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mencaine (lidocaine 4.5% Recalled by Wuhan Bingbing Pharmaceutical Co., Ltd....
The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Maximum Strength Lidocaine Cold & Hot Patch (lidocaine 4% Recalled by Wuhan...
The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LidoPatch (lidocaine HCl 3.6% Recalled by Wuhan Bingbing Pharmaceutical Co.,...
The Issue: CGMP Deviations: due to the loss of product manufacturing records and retain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips SureSigns VM1SpO2 Recalled by Philips North America, LLC Due to...
The Issue: Philips has identified a Philips SureSigns VM1 monitor in the possession of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mueller Knife Handle Recalled by Carefusion 2200 Inc Due to Becton Dickinson...
The Issue: Becton Dickinson and Company, is conducting a voluntary recall on the V....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.