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 1674116760 of 47,654 recalls

Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
FoodNovember 12, 2020· Tucson Tamale Wholesale Company, LLC

Recalled Item: Tucson Tamale Blue Corn & Veggie Tamales (2 Pack) Recalled by Tucson Tamale...

The Issue: Plastic pieces (1-2 cm) were discovered inside cans of tomatoes which were...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 12, 2020· Tucson Tamale Wholesale Company, LLC

Recalled Item: Tucson Tamale Blue Corn Recalled by Tucson Tamale Wholesale Company, LLC Due...

The Issue: Plastic pieces (1-2 cm) were discovered inside cans of tomatoes which were...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 12, 2020· Medtronic Inc.

Recalled Item: CareLink Personal Software Therapy Management Software Tool for Diabetes...

The Issue: Incomplete basal rate information may be transmitted leading to a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Medtronic Neuromodulation

Recalled Item: Medtronic Intellis Spinal Cord Stimulator Recalled by Medtronic...

The Issue: A710 Intellis Clinician Application has a software issue that can result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· ConMed Corporation

Recalled Item: Infinity ACL Tibial Tip Guide- indicated for use in open Recalled by ConMed...

The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· ConMed Corporation

Recalled Item: Infinity ACL Tibial Elbow Guide-indicated for use in open and Recalled by...

The Issue: Tips of the Infinity ACL Tibial Elbow and Tip Guides are potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Biocomposites, Ltd.

Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling

The Issue: The product is mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Hill-Rom Manufacturing, Inc.

Recalled Item: Life2000 Ventilation System Recalled by Hill-Rom Manufacturing, Inc. Due to...

The Issue: Under certain conditions, there is a risk for fire.

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

Class II — Potential Health HazardOngoing
DrugNovember 11, 2020· InvaTech Pharma Solutions, LLC

Recalled Item: Levocetirizine Dihydrochloride Tablets Recalled by InvaTech Pharma...

The Issue: Failed Impurities/Degradation Specifications: One lot of Levocetirizine...

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

Class III — Low RiskOngoing
Refund
DrugNovember 11, 2020· Apotex Corp.

Recalled Item: Aripiprazole Tablets Recalled by Apotex Corp. Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications: Out of specification for dissolution.

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2020· Teva Pharmaceuticals USA

Recalled Item: Testosterone Gel 1% Recalled by Teva Pharmaceuticals USA Due to Superpotent...

The Issue: Superpotent Drug: High out-of-specification assay results were obtained...

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

Class III — Low RiskOngoing
Refund
Medical DeviceNovember 11, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon PET-CT SCANNER Recalled by Canon Medical System, USA, INC. Due to A...

The Issue: A software problem has been identified which could result in the diagnostic...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: (Adult Elongated O2/CO2 Mask - Product Usage: intended Recalled by Westmed,...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Adult Elongated CO2/O2 Mask Recalled by Westmed, Inc. Due to There is a...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Recalled by Westmed, Inc. Due to There is a potential that the fitment...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2020· Westmed, Inc.

Recalled Item: Westmed DISPOSABLE RESPIRATORY PRODUCTS NON-REBREATHER MASK Recalled by...

The Issue: There is a potential that the fitment between the oxygen delivery tube and...

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

Class II — Potential Health HazardOngoing