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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 29241–29260 of 47,654 recalls
Recalled Item: CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit...
The Issue: The current secondary packaging, a box, incorrectly states that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoGuard Closed Luer Connector Recalled by B Braun Medical Inc Due to B....
The Issue: B. Braun is voluntarily recalling 13 lots of CytoGuard Closed Luer Connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMAG System Recalled by bioMerieux, Inc. Due to Some anomalies have been...
The Issue: Some anomalies have been identified during manufacturing controls.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...
The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Acetate 80 mg/mL Recalled by Isomeric Pharmacy Solution,...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate (Preservative Free) 20 mcg per mL (2 Recalled by PharMedium...
The Issue: Labeling: Not Elsewhere Classified- Diluent used to compound product expired...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...
The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate (Preservative Free) 10 mcg per mL (1 Recalled by PharMedium...
The Issue: Labeling: Not Elsewhere Classified- Diluent used to compound product expired...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenylephrine 2.5% Recalled by Isomeric Pharmacy Solution, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Acetate 40 mg/mL Recalled by Isomeric Pharmacy Solution,...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide 40 mg/mL Recalled by Isomeric Pharmacy Solution, LLC...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 200 mg/mL Recalled by Isomeric Pharmacy Solution, LLC...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estrone Recalled by Fagron, Inc Due to cGMP Deviations: lack of quality...
The Issue: cGMP Deviations: lack of quality assurance at the API manufacturer.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Diacetate 40 mg/mL Recalled by Isomeric Pharmacy Solution, LLC...
The Issue: Lack of Assurance of Sterility: due to concerns with production processes...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...
The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESTRONE Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...
The Issue: cGMP Deviations; manufacturer initiated recall of API product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.