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. 2,496 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,496 in last 12 months

Showing 2032120340 of 47,654 recalls

Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-Touch Screen Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: External Toco Transducer (M1355A) Recalled by Pacific Medical Group Inc. Due...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics RP-UI Assy Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco+ transducer with ECG/IUP capability (wired) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Tocotransducer (Nautilus) Recalled by Pacific Medical Group...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M2736A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Respironics California, LLC

Recalled Item: Respironics V680 Ventilator Recalled by Respironics California, LLC Due to...

The Issue: Ventilator touchscreen may become frozen and fail to respond to touch...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Roche Diagnostics cobas Integra Albumin Gen.2 Catalog Number: 05166861190 -...

The Issue: Due to low Quality Control recovery and invalid Calibration.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 11, 2019· Roche Diagnostics Operations, Inc.

Recalled Item: Cobas c Bilirubin Total Gen.3 Catalog Number: 05795419190 - Product Recalled...

The Issue: Due to low Quality Control recovery and invalid Calibration.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceSeptember 10, 2019· Novarad Corporation

Recalled Item: NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and...

The Issue: The firm received a report of an atypical dataset being generated. When...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products K+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· MEDTECH SAS

Recalled Item: Rosa Brain 3.0 Recalled by MEDTECH SAS Due to The instrument holder may be...

The Issue: The instrument holder may be sent on a trajectory that is not within the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 10, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Users may experience intermittent slide dispense issues with some cartridges...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2019· Exactech, Inc.

Recalled Item: Ergo 3.2mm K-wire - Product Usage: The devices is used Recalled by Exactech,...

The Issue: Potential for the wire to fracture at the threads and remain in the glenoid.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugSeptember 9, 2019· West-Ward Columbus Inc

Recalled Item: Oxcarbazepine Oral Suspension Recalled by West-Ward Columbus Inc Due to...

The Issue: Failed Impurities/Degradation Specificattion

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Darmerica, LLC

Recalled Item: Quinacrine Dihydrochloride (98.25%) Recalled by Darmerica, LLC Due to Label...

The Issue: Label Mix-Up: Product labeled as Quinacrine Dihydrochloride; however, after...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 6, 2019· Cardinal Health dba Specialty Pharmaceutical Services

Recalled Item: Nucala (mepolizumab) Injection Recalled by Cardinal Health dba Specialty...

The Issue: Temperature Abuse; Product stored and shipped outside of labeled storage...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2019· Torrent Pharma Inc.

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High Out Of Specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund