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. 1,067 recalls have been distributed to Virginia in the last 12 months.
Showing 16301–16320 of 29,425 recalls
Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MI Digital Ready Recalled by GE Healthcare, LLC Due to DIGITAL...
The Issue: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima CT 520 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard Complete Knee System Recalled by Zimmer Biomet, Inc. Due to Two...
The Issue: Two lots of tibial bearings were commingled. There is a possibility that a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revolution CT 160 1.5D STD WAUK Recalled by GE Healthcare, LLC Due to Some...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...
The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER Recalled...
The Issue: During long-term storage (i.e. military depot), the interaction of stagnant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CT Goldseal BrightSpeed 16 PWR TIO 2 YR Recalled by GE Healthcare, LLC Due...
The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Recalled by Steris...
The Issue: The firm has become aware that the Reliance 1227 Cart and Utensil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...
The Issue: This email is to provide notification that, due to a software bug that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANSYS TTC Recalled by NewDeal SA Due to Use of the impacted product may...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple...
The Issue: Device may be missing a sled component. The sled component is responsible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANSYS MLP/DLP Recalled by NewDeal SA Due to Use of the impacted product...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNI-CP Recalled by NewDeal SA Due to Use of the impacted product may cause a...
The Issue: Use of the impacted product may cause a superficial infection requiring PO...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.