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. 2,563 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,563 in last 12 months

Showing 9811000 of 27,884 recalls

Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 8" (20 cm) Ext Set w/MicroClave Clear Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 31" (79 cm) Appx 3.4 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock 13mm Closed Vial Spike Recalled by ICU Medical, Inc....

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 6" (15 cm) Ext Set w/MicroClave" Clear Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 73" (185 cm) Appx 2.5 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock w/Mini Bag Spike ¿ Recalled by ICU Medical, Inc. Due...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical Oncology Kit w/31" (79 cm) 20 Drop Admin Recalled by ICU...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 7.5" (19 cm) Appx 1.5 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Bag Spike with Clave Additive Port Recalled by ICU...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ChemoLock Bag Spike Recalled by ICU Medical, Inc. Due to Port weld of drug...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical 60" (152 cm) Appx 1.2 ml Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Vented Vial Spike Recalled by ICU Medical, Inc. Due to...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 8, 2025· ICU Medical, Inc.

Recalled Item: ICU Medical ChemoLock Universal Vented Vial Spike Recalled by ICU Medical,...

The Issue: Port weld of drug transfer device may separate or break during use and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2025· Iantrek Inc.

Recalled Item: Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300....

The Issue: Potential for compromised integrity of the sterile packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2025· Iantrek Inc.

Recalled Item: C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120....

The Issue: Potential for compromised integrity of the sterile packaging.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· Spacelabs Healthcare, Inc.

Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...

The Issue: Due to display cables used for monitors were not in compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 5, 2025· MICROVENTION INC.

Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....

The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...

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

Class II — Potential Health HazardOngoing