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. 914 recalls have been distributed to District of Columbia in the last 12 months.
Showing 42341–42360 of 47,654 recalls
Recalled Item: Portex¿ Spinal Tray with Drugs 22g Whitacre/25g Whitacre Recalled by Smiths...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Saddleblock Tray with Drugs 25g Quincke Recalled by Smiths Medical...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Saddleblock Tray with Drugs 22g Quincke (Without Introducer)...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano s5i/s5ix/s5iz/CORE Intravascular Ultrasound Imaging and Pressure...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ComboMap Intravascular Flow and Pressure System Recalled by Volcano Corp Due...
The Issue: A limitation in interoperability between the Philips Xper Flex Cardia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baylis Medical TorFlex Transseptal Guiding Sheath Recalled by Baylis Medical...
The Issue: The TorFlex Transseptal Guiding Sheath Kits are being recalled due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex¿ Spinal Tray with Drugs 25g Whitacre Recalled by Smiths Medical ASD,...
The Issue: Visual particulate in the glass ampules of 5% Lidocaine HCL and 7.5%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage¿ TOX Drug Screen Control 1 Product Generic Name: Recalled by...
The Issue: Alere San Diego, Inc. initiated a voluntary recall of Alere Triage TOX Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Next Choice" One Dose Emergency Contraceptive (Levonorgestrel Tablet)...
The Issue: Failed Tablet/Capsule Specifications: Multiple complaints for push through...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketoconazole Shampoo Recalled by Tolmar, Inc. Due to Subpotent
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...
The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irinotecan Hydrochloride Injection Recalled by West-Ward Pharmaceutical...
The Issue: Superpotent Drug: a recent review of the USP revealed that an incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEDRAD¿ Stellant CT Injector System with Certegra Workstation Recalled by...
The Issue: The root cause investigation showed that the under-volume hazard can occur...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultima OPCAB System Recalled by Maquet Cardiovascular, LLC Due to MAQUET has...
The Issue: MAQUET has identified a potential issue with the ULTIMA OPCAB (part numbers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)...
The Issue: The trial insertion instrument may disassemble during use due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Vantage Digital Panoramic System delivers high-value features standard...
The Issue: An error was identified in the Real Time Controller (RTC) firmware versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dairy Fresh Sour Cream Mac & Cheddar Recalled by Garden-Fresh Foods, Inc....
The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Weis Original Potato Salad Recalled by Garden-Fresh Foods, Inc. Due to...
The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Our Own Premium Potato Salad Recalled by Garden-Fresh Foods, Inc. Due to...
The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roundy's Dill Dip Recalled by Garden-Fresh Foods, Inc. Due to Potential...
The Issue: Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip...
Recommended Action: Do not consume. Return to store for a refund or discard.