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. 1,906 recalls have been distributed to Virginia in the last 12 months.
Showing 28261–28280 of 29,425 recalls
Recalled Item: Iris Diagnostics Division iQ Control/Focus Set Recalled by Iris Diagnostics...
The Issue: The firm initiated this recall because complaints from customers reported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...
The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareStream Dental Kodak 2100 Intraoral X-ray system Product Usage: The...
The Issue: There have been approximately 2% of the x-ray generators manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BariAir Therapy System The BariAir Therapy System is a risk Recalled by KCI...
The Issue: KCI has issued a medical device correction for the BariAir Therapy System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 400 system blood gas analyzer Product Usage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1260 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1245 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿ 500 system blood gas analyzer Product Usage: RAPIDPoint...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1240 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDLab¿ 1265 system blood gas analyzer Product Usage: RAPIDLab...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAPIDPoint¿¿ 405 system blood gas analyzer Product PUsage: These...
The Issue: RAPIDPoint¿ 400 Series, RAPIDPoint¿ 500, or RAPIDLab¿ 1200 Series blood gas...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS System versions 3.X and higher and 4.X and Recalled by Ge...
The Issue: There is a potential loss of image(s) associated with the Centricity to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Fluoroscan Mini C-Arm Model with InSight- FD Software Version...
The Issue: Fluoroscan Mini C-Arm models -InSight2, version 4.0 and 4.0.1 - DICOM images...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular AB Shells with Cluster Holes. The Trilogy Acetabular...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular Shells with Holes. The Trilogy Acetabular System is...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy F/M Acetabular Shell with Uni-Hole. The Trilogy Acetabular System...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Creatinine 120 CP Recalled by Horiba Instruments, Inc dba Horiba...
The Issue: This recall was initiated because some customers were experiencing an alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Acetabular AB Shells with Holes. The Trilogy Acetabular System...
The Issue: Some units of Trilogy shells manufactured since March 2009 may be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.