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. 2,537 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,537 in last 12 months

Showing 54415460 of 27,884 recalls

Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 29, 2023· Physio-Control, Inc.

Recalled Item: LIFEPAK 15 Recalled by Physio-Control, Inc. Due to Their is a potential for...

The Issue: Their is a potential for battery pins to become loose within the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2023· Olympus Corporation of the Americas

Recalled Item: TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP Recalled by Olympus Corporation...

The Issue: Fiberscopes do not have adequate data to support that the suction flow rate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2023· Boston Scientific Corporation

Recalled Item: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Recalled...

The Issue: Poor image quality due to fluid ingress in the lens.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2023· Boston Scientific Corporation

Recalled Item: EXALT Model D Single-Use Duodenoscope Recalled by Boston Scientific...

The Issue: Poor image quality due to fluid ingress in the lens.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2023· Medtronic Navigation, Inc.

Recalled Item: StealthStation S8 Application version 2.0 and 2.0.1 (Part 9735762) The...

The Issue: Due to a software anomaly which potentially could result in the surgical...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 27, 2023· Smith & Nephew, Inc.

Recalled Item: JOURNEY II BCS CONSTRAINED ARTICULAR INSERT Size 5-6 Recalled by Smith &...

The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2023· Smith & Nephew, Inc.

Recalled Item: JOURNEY II BCS ARTICULAR INSERT Recalled by Smith & Nephew, Inc. Due to The...

The Issue: The JRNY II BCS XLPE ART ISRT SZ 5-6 LT 10MM was laser etched, labeled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500 Blood Gas System Recalled by Siemens Healthcare Diagnostics...

The Issue: There are potential drug interferences from Perhexiline Maleate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: RAPIDPOINT 500e Blood Gas System Recalled by Siemens Healthcare Diagnostics...

The Issue: There are potential drug interferences from Perhexiline Maleate or...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: TERUMO 60" TUBE SET W/HIGH CRACK CHK VLV Recalled by B. Braun Medical, Inc....

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: THERASPHERE ADMIN SET Recalled by B. Braun Medical, Inc. Due to Devices may...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: 30 ML 2PORT BURETTE ASSEMBLY Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: AMO ADMINISTRATION SET Recalled by B. Braun Medical, Inc. Due to Devices may...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: 30ML BURETTE ASSY WITH STOPCOCK Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: ALLERGAN UNIVERSAL FILL KIT Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: FT1000S FLUID TRANSFER SET Recalled by B. Braun Medical, Inc. Due to Devices...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: SA3000 VENTED MICRO SPIKE ADAPTER Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 26, 2023· B. Braun Medical, Inc.

Recalled Item: BULK LARGEBORE MALE LL FITTING Recalled by B. Braun Medical, Inc. Due to...

The Issue: Devices may leak as a result of a manufacturing issue. Leakage may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 25, 2023· Olympus Corporation of the Americas

Recalled Item: Insufflation unit Recalled by Olympus Corporation of the Americas Due to...

The Issue: Olympus has become aware of an increased trend of both repairs and customer...

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

Class II — Potential Health HazardOngoing