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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.
Showing 37121–37140 of 47,654 recalls
Recalled Item: HEPARIN Sodium Injection USP Recalled by Pharmedium Services, LLC Due to...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 4 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 16 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: oxyTOCIN 15 Units added to 250 mL 5% Dextrose Injection USP Recalled by...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHrine HCl 1 mg added to 250 mL 0.9% Sodium Recalled by Pharmedium...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HEPARIN Sodium Injection USP 25 Recalled by Pharmedium Services, LLC Due to...
The Issue: Presence of Particulate Matter: The firm produced products using 0.9% Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Capsules USP Recalled by Teva Pharmaceuticals USA Due to Chemical...
The Issue: Chemical Contamination: Product recalled due to an elevated level of a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Inj. USP Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...
The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: Study and all acquired images deleted when using systems with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...
The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...
The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...
The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.