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. 2,807 recalls have been distributed to Virginia in the last 12 months.
Showing 8341–8360 of 53,829 recalls
Recalled Item: AU/DxC AU Chemistry Transferrin Immune complexes formed in Recalled by...
The Issue: The firm has identified that the Transferrin reagent does not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Modena-IVD Clinical Chemistry Analyser Catalog Number: RX9000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Monaco-IVD Clinical Chemistry Analyser Catalog Number: RX5000 Recalled by...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Imola-IVD Clinical Chemistry Analyzer Catalog Number: RX4900. RX4900R ()...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (with ISE)-IVD Clinical Chemistry Analyser Catalog Number:...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041...
The Issue: RX Parameter rerun settings (Sample Volume Low/High), and Dilutions used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX BLUESTAR Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis SYS Recalled by Fresenius Medical Care Holdings, Inc. Due...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. W/O CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System w/Bibag Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T GEN 2 Bibag without CDX Recalled by Fresenius Medical Care Holdings,...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX W/BIBAG BLUESTAR Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T Hemodialysis System without CDX Recalled by Fresenius Medical Care...
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis CII Safe ES Recalled by CareFusion 303, Inc. Due to When global...
The Issue: When global edit is used to update multiple formulary properties...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HD SYS. CDX BLUESTAR Recalled by Fresenius Medical Care Holdings, Inc....
The Issue: Potential PCBA leaching from tubing of hemodialysis machines.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL...
The Issue: Some Venue Go Standard Carts can develop an internal failure of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Meera Mobile Operating Table-to support and position the patient immediately...
The Issue: Under certain conditions, an issue might prevent the device from performing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection 40mg per vial Recalled by BE...
The Issue: Lack of Assurance of Sterility: Powder discoloration due to small crack in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atrium Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Product was re-processed and re-sterilized by a third party using packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Oasis Dry Suction Water Seal Chest Drain Recalled by Atrium Medical...
The Issue: Product was re-processed and re-sterilized by a third party using packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.