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. 2,616 recalls have been distributed to District of Columbia in the last 12 months.
Showing 8941–8960 of 47,654 recalls
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGACY SMARTBASE Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Non-engaging abutments were distributed without FDA clearance; the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith&Nephew ENGAGE Cementless Partial Knee System Recalled by Smith &...
The Issue: Recent complaint data indicates that the revision rate may be trending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Sign Sensor 2 Recalled by SenTec AG Due to The sensors may experience an...
The Issue: The sensors may experience an out-of-box failure because after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Universal Ventilator Recalled by Philips Respironics, Inc. Due...
The Issue: The Trilogy Evo Universal ventilator provides continuous or intermittent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 EV300 Recalled by Philips Respironics, Inc. Due to...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Recalled by...
The Issue: IFU- Instructions for Use (IFU) package insert and both the IFU packaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Environmental...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 and LifeVent EVO2 Recalled by Philips Respironics, Inc. Due...
The Issue: Environmental debris may accumulate on the internal machine flow sensor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Famotidine Tablets Recalled by Glenmark Therapeutics, Inc. Due to Labeling:...
The Issue: Labeling: Label Error on Declared Strength: some cartons labeled and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Copitas Recalled by Pernod Ricard Usa Inc Due to Product may exceed FDA...
The Issue: Product may exceed FDA guidance levels for leachable lead.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: vasopressin 20 units added to 0.9% sodium chloride 100 mL* Recalled by...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neonatal TPN Starter Bag Recalled by Central Admixture Pharmacy Services,...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardioplegia Solution Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MSA 7.84% MSG 8.56% (0.92M) Comp. Sol. 1000 ml bag Recalled by Central...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: vancomycin added to 0.9% sodium chloride Recalled by Central Admixture...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: diphenhydrAMINE 50 mg added to 0.9% sodium chloride 50 mL Recalled by...
The Issue: Lack of Assurance of Sterility: after an FDA inspection called into question...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.