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. 969 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
969 in last 12 months

Showing 26201–26220 of 48,376 recalls

FoodFebruary 5, 2018· eBars

Recalled Item: FIT ORGANIC PEANUT BUTTER CHOCOLATE RASPBERRY bar NET WT 1.8 Recalled by...

The Issue: The firm was notified by the State of TN that the product contained...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: HEAL ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...

The Issue: The product test positive for almond allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: RUN ORGANIC CHOCOLATE ALMOND bar NET WT. 1.6 OZ (45g) Recalled by eBars Due...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: FOCUS ORGANIC CHOCOLATE PEANUT bar NET WT. 1.6 OZ (45g) Recalled by eBars...

The Issue: The firm was notified by the State of TN that the product contained...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 5, 2018· eBars

Recalled Item: GOLF ORGANIC CHOCOLATE ALMONDS bar NET WT. 1.6 OZ (45g) Recalled by eBars...

The Issue: The product test positive for peanut allergen which is not declared on the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2018· 3M Company - Health Care Business

Recalled Item: 3M Surgical Clipper Professional 9681 Recalled by 3M Company - Health Care...

The Issue: Failure to follow proper charging practices can result in lithium-ion...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Signature Orthopedics Pty Limited

Recalled Item: Signature Ceramic Femoral Head. Model Number: 111-152-621. The Signature...

The Issue: This recall has been identified due to the batch being mislabeled, with the...

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

Class II — Potential Health HazardOngoing
DrugFebruary 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Metformin Hydrochloride Tablets Recalled by Aurobindo Pharma Ltd. Due to...

The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was found in bottle of...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 2, 2018· ALLERGAN

Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets Recalled by...

The Issue: Labeling: Not Elsewhere Classified: does not have the required "CII"...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Merit Medical Systems, Inc.

Recalled Item: 1mL Medallion Syringes Are used to inject fluids into Recalled by Merit...

The Issue: Supplier manufacturing defect with the syringe plunger tip.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 1000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 100 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 2000 Recalled by Shippert Medical Technologies Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans Syringe Fill 360 Recalled by Shippert Medical Technologies Due...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2018· Shippert Medical Technologies

Recalled Item: Tissu-Trans FILTRON 250 Recalled by Shippert Medical Technologies Due to The...

The Issue: The pouch integrity of the sterile product can't be assured without a visual...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Spirit(Model 10045692 ) Recalled by Siemens Medical Solutions USA,...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Medline Industries Inc

Recalled Item: Medline 0.9 % Sodium Chloride Injection Recalled by Medline Industries Inc...

The Issue: Packaged with an incorrect overwrap.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Emotion 6 (Model 10165888) Recalled by Siemens Medical Solutions...

The Issue: A potential risk of unnecessary radiation exposure due to a software issue

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

Class II — Potential Health HazardOngoing