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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,542 in last 12 months

Showing 1822118240 of 47,654 recalls

DrugMay 13, 2020· West-Ward Columbus Inc

Recalled Item: Ethacrynic Acid Tablets USP Recalled by West-Ward Columbus Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· DiaSorin Molecular LLC

Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...

The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2020· Med Tec Inc

Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...

The Issue: Potential for disengagement of the Varian Style Type-S Extension during...

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

Class II — Potential Health HazardOngoing
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) + Curcumin 50mg/mL Recalled by BIOTA Biosciences...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Curcumin 50mg/mL Recalled by BIOTA Biosciences LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Curcumin Recalled by BIOTA Biosciences LLC Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) 4mg/mL Recalled by BIOTA Biosciences LLC Due to...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· BIOTA Biosciences LLC

Recalled Item: Sterile Cannabidiol (CBD) 50mg/mL Recalled by BIOTA Biosciences LLC Due to...

The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 11, 2020· Torrent Pharma Inc.

Recalled Item: Carbamazepine Tablets Recalled by Torrent Pharma Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX CO-OX 393-841 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Radiometer Medical ApS

Recalled Item: ABL80-FLEX-393-839 Box Label Recalled by Radiometer Medical ApS Due to...

The Issue: Barcode readers on ALB900 and ABL800 analyzers used for measuring pH, blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier I Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product Performance Verifier II Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Product AMYL Slides Reagent Recalled by Ortho-Clinical...

The Issue: Multiple coatings of VITROS Chemistry Products AMYL Slides are showing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 11, 2020· Biomet, Inc.

Recalled Item: Comprehensive VRS Inserter Recalled by Biomet, Inc. Due to The product is...

The Issue: The product is being recalled due to the central screw drill seizing inside...

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

Class II — Potential Health HazardOngoing
DrugMay 8, 2020· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...

The Issue: Presence of Particulate Matter: confirmed customer complaint for the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 8, 2020· Ge Healthcare

Recalled Item: The OEC 9900 C-Arm is designed to provide fluoroscopic and Recalled by Ge...

The Issue: GEHC Surgery became aware that some users of the 9800 and 9900 fluoroscopic...

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

Class II — Potential Health HazardOngoing