Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,997 recalls have been distributed to Virginia in the last 12 months.
Showing 14721–14740 of 29,425 recalls
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Recalled by Integra LifeSciences Corp. Due to The Salto...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 Recalled by Becton...
The Issue: BD PAS received customer complaints indicating the absence of the bevel on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity ci-series System Control Module software version 2.5.1...
The Issue: Potential performance issues in the Alinity-ci software version 2.5.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to Potential...
The Issue: Increased risk of false positive Enterobacteriaceae and Escherichia coli...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel Recalled by BioFire Diagnostics, LLC...
The Issue: Elevated rates of false positive results for Campylobacter and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AquaBeam Handpiece Recalled by PROCEPT BIOROBOTICS CORPORATION Due to...
The Issue: Certain lots may develop an internal leak due to a micro-crack in a specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Kabi CATSmart device (Continuous autotransfusion System). Labeled...
The Issue: Based on internal investigations, Fresenius Kabi has identified a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07...
The Issue: The firm has initiated a recall due to a confirmed complaint trend for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07...
The Issue: The firm has initiated a recall due to a confirmed complaint trend for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System Recalled by...
The Issue: Leak from the septum assembly or the canister may burst under high pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thoratec HeartMate 3 Coring Tool Recalled by Thoratec Corp. Due to Small...
The Issue: Small black plastic particle was observed in the left ventricle during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra bioBLOCK Resorbable subtaler Implant Recalled by Integra Limited Due...
The Issue: Temperature indicator may have changed color to dark gray or black prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.