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. 2,356 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,356 in last 12 months

Showing 2650126520 of 48,376 recalls

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: 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 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
DrugDecember 14, 2017· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: SPIRIVA HandiHaler (tiotropium bromide inhalation powder) 18 mcg/capsule (90...

The Issue: Failed Stability Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Universal Defense SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Discovery Set contains SPF 50+ (octinoxate 4.9%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion (zinc oxide 23.8%...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solution LX Luxurious Eye & Lip Collection contains Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· SHISEIDO AMERICA INC.

Recalled Item: Shiseido Future Solutions LX Triple Points Bonus contains SPF 50+ Recalled...

The Issue: GMP Deviations: manufacturing of API material did not meet GMP and quality...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 14, 2017· Teva Pharmaceuticals USA

Recalled Item: Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP Recalled by...

The Issue: Failed Impurities/Degradation Specifications: High out of specification test...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 13, 2017· ALLERGAN

Recalled Item: INFeD (Iron Dextran Injection USP) 100 mg elemental iron/2 ml (50 mg/mL)...

The Issue: Failed Stability Specifications: Product stability testing results did not...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
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
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
DrugDecember 12, 2017· Keryx Biopharmaceuticals, Inc.

Recalled Item: Auryxia (ferric citrate) tablets Recalled by Keryx Biopharmaceuticals, Inc....

The Issue: Presence of Foreign Substance: Reports have been received of damaged...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Rachael's SPRINGFIELD SMOKED FISH LOX CREAM CHEESE SPREAD Recalled by...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Boston Salads Scallion Cream Cheese Spread Recalled by Rachael's Food...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: SPRINGFIELD SMOKED FISH Smoked Bluefish Recalled by Rachael's Food...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodDecember 12, 2017· Rachael's Food Corporation

Recalled Item: Rachael's SPRINGFIELD SMOKED FISH Smoked Trout 6 oz Recalled by Rachael's...

The Issue: Product may be contaminated with Listeria monocytogenes.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund