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. 2,373 recalls have been distributed to District of Columbia in the last 12 months.
Showing 43321–43340 of 47,654 recalls
Recalled Item: VITROS Chemistry Products Ca Slides packaged as 300 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arm & Hammer Baking Soda a) Net Wt. 1 LB. Recalled by Church & Dwight Inc...
The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Pistachios Recalled by Hearthside Food Solutions LLC Due to One of our...
The Issue: One of our vendors, ARO Pistachio Inc., is issuing an FDA Class 2 Voluntary...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sodium Bicarbonate Recalled by Church & Dwight Inc Due to Church and Dwight...
The Issue: Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Medullary Reamer. Intended to be used to facilitate...
The Issue: Due to the coiled design for this product, the product is difficult to clean...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigliani/Flatow¿ The Complete Shoulder Solution Recalled by Zimmer, Inc. Due...
The Issue: The firm is initiating a removal of one lot of the Bigliani/Flatow Humeral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate Powder Recalled by Church & Dwight Inc Due to Presence of...
The Issue: Presence of Foreign Substance: raw material recalled due to stainless steel...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bethel 30 capsules Recalled by Bethel Nutritional Consulting, Inc Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare MobileDiagnostwDR system. Mobile Digital radiography...
The Issue: The Instructions for Use (IFU) for the MobileDiagnost wDR fails to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: GE has recently become aware of potential issues due to out of context...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring Recalled by Integra...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Recalled by...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inegra Licox Brain Tissue Oxygen Monitoring 1 x Complete Brain Recalled by...
The Issue: Integra LifeSciences Corporation has determined that there is a possibility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.