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. 2,525 recalls have been distributed to West Virginia in the last 12 months.

48,376 total recalls
2,525 in last 12 months

Showing 92619280 of 48,376 recalls

Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 14, 2023· Mechatronics USA

Recalled Item: RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml Recalled by...

The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....

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

Class III — Low RiskOngoing
Medical DeviceApril 14, 2023· Mechatronics USA

Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...

The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....

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

Class III — Low RiskOngoing
Medical DeviceApril 14, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...

The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...

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

Class II — Potential Health HazardOngoing
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-200 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel DG Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-102 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
DrugApril 13, 2023· DuPont Nutrition USA, Inc

Recalled Item: Avicel PH-101 NF Recalled by DuPont Nutrition USA, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class III — Low RiskOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: Gelson's Sea Salt Pretzels Recalled by Dakota Style, Inc Due to Undeclared Milk

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Salt & Vinegar Braided Pretzels Recalled by Dakota Style, Inc Due...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Dill Pickle Braided Pretzels Recalled by Dakota Style, Inc Due to...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 13, 2023· Dakota Style, Inc

Recalled Item: 1. Hy-Vee Honey Mustard Braided Pretzels Recalled by Dakota Style, Inc Due...

The Issue: May contain undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...

The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· Howmedica Osteonics Corp.

Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...

The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2023· TELEFLEX LLC

Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...

The Issue: The product contains an expired diluent vial. If the impacted product is...

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

Class II — Potential Health HazardOngoing