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. 2,372 recalls have been distributed to West Virginia in the last 12 months.
Showing 23061–23080 of 48,376 recalls
Recalled Item: Fentanyl Citrate 2 mcg per mL (200 mcg per 100 Recalled by Pharmedium...
The Issue: Sub-potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 2 mcg per mL (100 mcg per 50 Recalled by Pharmedium...
The Issue: Sub-potent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Toothete Oral Care Sodium Bicarbonate Mouthpaste Recalled by Sage Products...
The Issue: A voluntary recall of a lot (67924) of Independent Care System due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...
The Issue: The sterility may be compromised due to a potential breach in the packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 660i Recalled by Beckman Coulter Inc. Due to When racks are...
The Issue: When racks are front-loaded onto the sample presentation unit while samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UniCel DxI 600 and 800 Access Immunoassay Systems Recalled by Beckman...
The Issue: When racks are front-loaded onto the sample presentation unit while samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...
The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol Tablets Recalled by Epic Pharma, LLC Due to Presence of foreign...
The Issue: Presence of foreign tablet/capsule: A single foreign tablet was found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diatomaceous Earth packaged in the following ways: 1) Perma-Guard Recalled...
The Issue: Product contains elevated levels of lead, arsenic, and chromium: potentially...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROOT 23 CUCUMBER HABANERO SIMPLE SYRUP 375 ml Recalled by Root 23 LLC Due to...
The Issue: Non-compliance with process authority schedule; temperature at start of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox CALCIUM (Ca) Colorimetric Method RX Series Cat. No. CA 3871 Recalled...
The Issue: Update to the carryover avoidance technical bulletin to introduce additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox CALCIUM (Ca) COLORIMETRIC METHOD RX DAYTONA PLUS Cat. No. CA 8309 R1...
The Issue: Update to the carryover avoidance technical bulletin to introduce additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...
The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fructosamine Control 3 Recalled by Randox Laboratories Ltd. Due to The firm...
The Issue: The firm is conducting a Device Modification for Fructosamine Calibrator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fructosamine Calibrator Recalled by Randox Laboratories Ltd. Due to The firm...
The Issue: The firm is conducting a Device Modification for Fructosamine Calibrator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fructosamine Control 1 Recalled by Randox Laboratories Ltd. Due to The firm...
The Issue: The firm is conducting a Device Modification for Fructosamine Calibrator,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.