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 16881–16900 of 47,654 recalls
Recalled Item: Olanzapine Orally Disintegrating Tablets Recalled by Jubilant Cadista...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer - Product Usage: automated Recalled by Siemens...
The Issue: Test Definition scanning may reset custom settings to defaults. When a 2D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Felodipine Extended Release Tablets Recalled by Heritage Pharmaceuticals Inc...
The Issue: Failed impurities/ degradation specifications: Out of specification impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by Nostrum...
The Issue: CGMP Deviations: detection of N-Nitrosodimethylamine (NDMA) impurity above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Viral Transport Medium Recalled by Hardy Diagnostics Due to There is a...
The Issue: There is a potential for contamination within Viral Transport Media. Use of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO System. With the following model numbers: a. EVOLUTPRO-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) PRO+ System. With the following model numbers: a. Recalled by...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evolut (TM) R System. With the following model numbers: a. EVOLUTR-23...
The Issue: Potential for Transcatheter Aortic Valve (TAV) leaflet damage when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Biomeme SARS-CoV-2 Real-Time RT-PCR Test is a molecular in Recalled by...
The Issue: The firm has become aware of nine reports by a single customer that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Pen Needles 32G x 4mm (5/32' )-intended for Recalled by Becton...
The Issue: Product shelf cartons incorrectly labeled as products intended for the Latin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Box Label: ION Fully Articulating Catheter Recalled by Intuitive Surgical,...
The Issue: The distal tip ring of the fully articulating catheter may become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Pump - Product Usage: indicated for male patients suffering Recalled...
The Issue: Potential increased occurrence of pump fracture over the lifetime of the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mako Integrated Cutting System (MICS) Handpiece Recalled by Mako Surgical...
The Issue: Stryker has discovered a characterization issue associated with the Mako...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vapor Ointment packaged in a) 1/8 oz Recalled by H & H Remedies, LLC Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: White Liniment packaged in a) 1 oz Recalled by H & H Remedies, LLC Due to...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Union (black) salve packaged in a) 1/8 oz Recalled by H & H Remedies, LLC...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chef Myron's Szechuan Sauce Recalled by JMH International, LLC Due to...
The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chef Myron's Tangy Teriyaki Sauce Recalled by JMH International, LLC Due to...
The Issue: Product utilized a gluten-free claim but has as an ingredient a fermented...
Recommended Action: Do not consume. Return to store for a refund or discard.