Product Recalls in West Virginia

Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,005 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,005 in last 12 months

Showing 35013520 of 27,884 recalls

Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Desc: Product Name: A-OK 19G V-LANCE FULL HANDLE1.6MM SATIN Recalled...

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· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 7.5CPM Recalled by Alcon Research LLC Due to Alcon...

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· Omnia Medical

Recalled Item: TiBrid Stand Alone Intervertebral Body Fusion Device Recalled by Omnia...

The Issue: Failure of fusion system instruments in the field.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2024· Alcon Research LLC

Recalled Item: Product Name: 25+ CMB PAK 10K CPM Recalled by Alcon Research LLC Due to...

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· Alcon Research LLC

Recalled Item: Product Desc: Product Name: CLEARCUT SAFETY INTREPID DB Recalled by Alcon...

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· Alcon Research LLC

Recalled Item: Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106...

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 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· 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· 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