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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.

47,654 total recalls
2,639 in last 12 months

Showing 34813500 of 27,451 recalls

Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SB INTREPID 2.2 ANG Model/Catalog...

The Issue: Alcon has detected an increase in complaint reports related to sharpness for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Software...

The Issue: Potential Loss of Imaging (X-ray) Functionality and/or Longer Time to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Meddev Corp

Recalled Item: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog...

The Issue: Due to mislabeling of products

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 7100 Recalled by Datex-Ohmeda, Inc. Due to Potential issue that may...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys CS2 with Et Control. This anesthesia gas machine is Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 100. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Avance CS2 and Avance CS2 Pro. These anesthesia gas machines Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aisys. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Avance. This anesthesia gas machine is intended to provide general Recalled...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Amingo. OUS only. Recalled by Datex-Ohmeda, Inc. Due to Potential issue that...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire 7900. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Datex-Ohmeda, Inc.

Recalled Item: Aespire View. This anesthesia gas machine is intended to provide Recalled by...

The Issue: Potential issue that may arise if the limb of a patient breathing circuit is...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 12, 2024· Intuitive Surgical, Inc.

Recalled Item: Ion Endoluminal System Recalled by Intuitive Surgical, Inc. Due to There is...

The Issue: There is a potential that the robotic system's instrument cart arm may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 12, 2024· LINEAGE BIOMEDICAL, INC

Recalled Item: NavaClick Syringe and Needle Recalled by LINEAGE BIOMEDICAL, INC Due to...

The Issue: Incorrect GTIN number on carton.

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

Class III — Low RiskOngoing
Medical DeviceJuly 10, 2024· Beckman Coulter, Inc.

Recalled Item: Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman...

The Issue: Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2024· Bard Peripheral Vascular Inc

Recalled Item: Guidewire 70cm x 1mm (0.038 ) These accessories Recalled by Bard Peripheral...

The Issue: Due to guidewires being manufactured incorrectly with the guidewires being...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2024· Beckman Coulter Mishima K.K.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Mishima...

The Issue: Due to a software issues, after the instrument processes 250 racks...

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

Class II — Potential Health HazardOngoing