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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,552 in last 12 months

Showing 1602116040 of 47,654 recalls

Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System...

The Issue: Due to not having the full complement of biological assessments for all...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: PRECICE PLATE - Product Usage: intended for limb lengthening Recalled by...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: PRECICE STRYDE - Product Usage: intended for limb lengthening Recalled by...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Nuvasive Specialized Orthopedics Inc

Recalled Item: Precice Bone Transport - Product Usage: intended for limb lengthening...

The Issue: Due to complaints of adverse events potentially related to biological...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· TELEFLEX MEDICAL INC

Recalled Item: PLEUR-EVAC Thoracic Catheters (CATHETER Recalled by TELEFLEX MEDICAL INC Due...

The Issue: Teleflex is recalling this product due to a lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro...

The Issue: VITROS Immunodiagnostic Products SARS-CoV-2 Antigen False Reactive Results...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2021· Medtronic Vascular, Inc.

Recalled Item: Valiant Navion Thoracic Stent Graft System. For endovascular repair of...

The Issue: Due to the presence of type IIIb endoleaks, stent fractures, and stent ring...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 11, 2021· Hollister Incorporated

Recalled Item: Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and...

The Issue: The tube holder can separate from the barrier that secures the device to the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Metoclopramide Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Sterile Diluent for Epoprostenol Sodium for Injection Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Desmopressin Acetate Injection USP Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Dacarbazine for Injection USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Vecuronium Bromide for Injection Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: MethyIPREDNISolone Acetate Injectable Suspension USP Recalled by Teva...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Toposar (etoposide injection USP) Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 10, 2021· Teva Pharmaceuticals USA

Recalled Item: Epoprostenol Sodium for Injection Recalled by Teva Pharmaceuticals USA Due...

The Issue: Lack of Assurance of Sterility: manufacturing areas for the recalled...

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

Class II — Potential Health HazardOngoing
Refund