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. 2,266 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,266 in last 12 months

Showing 4552145540 of 48,376 recalls

Medical DeviceFebruary 26, 2013· Cooper Surgical, Inc.

Recalled Item: Cooper Surgical Gellhorn Flexible Pessary 3" Recalled by Cooper Surgical,...

The Issue: Pessary mislabeled outer package may not the size of the product contained...

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

Class III — Low RiskOngoing
Medical DeviceFebruary 26, 2013· Neurotherm, Inc.

Recalled Item: Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge Recalled by...

The Issue: Straight needle labeled as a curved needle

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

Class II — Potential Health HazardOngoing
DrugFebruary 26, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Cefdinir for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Defective Container: This recall is being carried out due to the potential...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Furosemide Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: QUELICIN (succinylcholine chloride) Injection Recalled by Hospira Inc. Due...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Hospira Inc.

Recalled Item: Sodium Acetate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 26, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Lisinopril Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Tablets/Capsules Imprinted With Wrong ID: Pharmaceuticals are imprinted with...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 26, 2013· Giant Eagle

Recalled Item: Giant Eagle Lotsa Chocolate Chip Cookies Recalled by Giant Eagle Due to...

The Issue: Labels do not accurately state ingredients/nutrition facts/allergens. An...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog #...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nipro Diagnostics, Inc.

Recalled Item: Duane Reade TRUEtrack monitor kit Recalled by Nipro Diagnostics, Inc. Due to...

The Issue: Meter kit outer boxes containing 10 ct. test strips state incorrect storage...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Select Control Solution Recalled by Lifescan Inc...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Symbios Medical Products, LLC

Recalled Item: GOPump Elastometric infusion PumpKit with/ and without accesssories all...

The Issue: Received 2 complaints out of 458 distributed pumps in this lot, where flow...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 25, 2013· Nova Biomedical Corporation

Recalled Item: Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214...

The Issue: Glucose test strips reports no result message when tested

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Lifescan Inc

Recalled Item: LifeScan brand OneTouch¿ Ultra Control Solution Recalled by Lifescan Inc Due...

The Issue: When OneTouch¿ Ultra and OneTouch¿ Select test strips are tested with Ultra...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: CAPD Solution Transfer Set with Locking Connector. Product Code: 5C4160....

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set. Product Code 5C4449. intended...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set (6") with Twist Clamp. Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2013· Baxter Healthcare Corp.

Recalled Item: MiniCap Extended Life PD Transfer Set Extra Short (4") with Recalled by...

The Issue: Labeling Revision: Additional instructions for the use of peritoneal...

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

Class II — Potential Health HazardOngoing
DrugFebruary 25, 2013· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Visible particulate embedded in vials was...

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

Class II — Potential Health HazardOngoing
Refund