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. 2,460 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,460 in last 12 months

Showing 1644116460 of 27,884 recalls

Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: iView DAB IHC Detection Kit Recalled by Ventana Medical Systems Inc Due to...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: NEXES VEN IVIEW DAB DET KT JPN-US EXPORT Recalled by Ventana Medical Systems...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 19, 2017· Ventana Medical Systems Inc

Recalled Item: CINtec PLUS Cytology Kit (Canada/Japan) Recalled by Ventana Medical Systems...

The Issue: Increased reports of leaking and sticking reagent dispensers for horseradish...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: Modular E 170 Analyzer: Immunoassay Chemistry Analyzer Recalled by Roche...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: c6000 Recalled by Roche Diagnostics Corporation Due to Complaints have been...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur BNP (B-type Natriuretic Peptide) Recalled by Siemens...

The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c5 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c5, Ampicilloyl were not met.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur TSH3-Ultra (Thyroid Stimulating Hormone 3 Ultra) Recalled by...

The Issue: In certain scenarios the ADVIA Centaur CP, XP and XPT immunoassay analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Phadia US Inc

Recalled Item: ImmunoCAP Allergen c6 Recalled by Phadia US Inc Due to The stability...

The Issue: The stability specifications of ImmunoCAP Allergen c6, Amoxicilloyl were not...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Roche Diagnostics Corporation

Recalled Item: cobas e 411 Immunoassay Analyzer (Discrete Photometric Analyzer for Clinical...

The Issue: Complaints have been received concerning questionable results on analyzers...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS for ASTIGMATISM Brand Contact Lenses. Lot no. B00NKM0G....

The Issue: Package integrity failure observed during routine shift package integrity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor -Monica IF24 Interface System Product...

The Issue: if the cables of the Monica IF24 System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· GE Healthcare, LLC

Recalled Item: Uterine Electromyographic Monitor - Monica Novii Wireless Patch System...

The Issue: if the cables of the Monica Novii System are removed by a user, and then...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView Model 882480 Product Usage: BrightView and BrightView X are...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 6 Model # 882351 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView XCT Model 882482 Product Usage: BrightView XCT is a Recalled by...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Precedence 16 Model # 882350 Product Usage: Precedence (cleared as Recalled...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: BrightView X Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: During collimator exchange, the alignment of the collimator cart and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2017· Covidien LLC

Recalled Item: Signia" Power Handle (SIGPHANDLE Recalled by Covidien LLC Due to Product...

The Issue: Product reportedly shutting down during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 13, 2017· Halyard Health, Inc

Recalled Item: CORTRAK* 2 Nasogastric/Nasointestinal (NG/NI) Feeding Tubes with...

The Issue: The transmitting stylet within CORTRAK* 2 nasogastric/Nasointestinal (NG/NI)...

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

Class II — Potential Health HazardOngoing