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. 2,521 recalls have been distributed to West Virginia in the last 12 months.
Showing 9441–9460 of 27,884 recalls
Recalled Item: Cytocell LPH019-A E2A (TCF3) Breakapart Probe- In Vitro Diagnostic Analyte...
The Issue: May show unexpected locus specific signals in addition to those at 19p13.3....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...
The Issue: The devices have a different inner diameter than the diameter specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann SCS Screwdriver Recalled by Straumann USA LLC Due to Tip of the...
The Issue: Tip of the screwdriver does not have the correct configuration / profile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nail Insertion Sleeve Recalled by Stryker GmbH Due to The devices have a...
The Issue: The devices have a different inner diameter than the diameter specified on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60...
The Issue: Telepack may not power on when using the 3AA battery cradle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno- angiography systems developed for single and biplane diagnostic...
The Issue: Software error VE10B -In case of a fault within the drivetrain of an axis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R1.x Recalled by PHILIPS MEDICAL...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion systems with software release R2.0.x Recalled by Philips Healthcare...
The Issue: In the Azurion system, the user can add a new study to a patient by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unifine Pentips Plus Recalled by Owen Mumford USA, Inc. Due to Mixed Up. Two...
The Issue: Mixed Up. Two (2) cases of Unifine Pentips Plus 4mm pen needles have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave 3 cc/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC Due...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards VAMP Jr. 6 in (15 cm) Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Recalled by Edwards Lifesciences, LLC Due to There is a potential...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr Recalled by Edwards Lifesciences, LLC Due to...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr Kit Recalled by Edwards Lifesciences, LLC...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit Recalled by Edwards...
The Issue: There is a potential that the pressure tubing may detach from the blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Physician Order Form (PL-15400-00 Recalled by Flowonix Medical Inc Due to...
The Issue: Physician Order Form (PL-15400-00 Nov 2018) distributed is discontinued due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cotton Rounds/Pads under the following brand names: 1. BEAUTY 360 Recalled...
The Issue: Potential for mold contamination (Aspergillus vadensis)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tempus Pro - Patient physiological monitor Recalled by Remote Diagnostic...
The Issue: The Tempus Pro (Trizeps 7 only) when used in combination with a specified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.