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. 2,411 recalls have been distributed to District of Columbia in the last 12 months.
Showing 39401–39420 of 47,654 recalls
Recalled Item: Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate)...
The Issue: Presence of Foreign Substance: Truvada was found to contain small red...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: Certain lots of the reagent cartridges show confirmed positive bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...
The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...
The Issue: Packaging of a device was compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...
The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...
The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASTS-LG1212: Anterior Lumbar Interbody Fusion Spine Truss System (orthopedic...
The Issue: Product is mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...
The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DOPamine Hydrochloride and 5% Dextrose INJ Recalled by Baxter Healthcare...
The Issue: Lack of Assurance of Sterility: A small cut in the solution bag may have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium and Misoprostol Delayed-Release Tablets Recalled by...
The Issue: Failed Tablet/Capsule Specifications: Presence of split or broken tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bystolic (nebivolol) tablets Recalled by Forest Pharmaceuticals Inc Due to...
The Issue: Failed Dissolution Specification; at the 6-month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Sun Pharma...
The Issue: Failed Dissolution Specifications; 12 month stability time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merit Maestro Microcatheter Recalled by Merit Medical Systems, Inc. Due to...
The Issue: These microcatheters were packaged with a 2.8 F distal tip, rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Calibrator E Recalled by Siemens Healthcare Diagnostics, Inc Due to...
The Issue: Positive bias for Calibrator E lot kits ending in 38 and 39 with the ADVIA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotome Biopsy Needle Set...
The Issue: MEDINVENTS, the manufacturer of the Spirotome" Soft-Tissue Biopsy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...
The Issue: An investigation identified that high level friction may exist between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Green Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...
The Issue: An investigation identified that high level friction may exist between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.