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. 1,983 recalls have been distributed to Virginia in the last 12 months.
Showing 16881–16900 of 29,425 recalls
Recalled Item: ST-AIA PACK TT3 Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part no. 690.380 Recalled by Synthes (USA) Products LLC Due to Affected...
The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK PAP Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK cTnI 2nd Gen Recalled by Tosoh Bioscience Inc Due to Asfotase...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh ST AIA-PACK HbA1c Recalled by Tosoh Bioscience Inc Due to The assay...
The Issue: The assay can potentially generate erroneously elevated or erroneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK Estradiol Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part no. 690.379 Recalled by Synthes (USA) Products LLC Due to Affected...
The Issue: Affected screw gauges incorrectly measure screws 5.41mm shorter than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tosoh ST AIA-PACK HbA1c Calibrator Recalled by Tosoh Bioscience Inc Due to...
The Issue: The assay can potentially generate erroneously elevated or erroneously...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK BMG Recalled by Tosoh Bioscience Inc Due to Asfotase Alfa...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST-AIA PACK C-Peptide II Recalled by Tosoh Bioscience Inc Due to Asfotase...
The Issue: Asfotase Alfa (Strensiq) interferes with certain Tosoh assays which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flex Arm Product Usage: The Synthes Flex Arm is a Recalled by Synthes, Inc....
The Issue: Quick connect feature of instruments may be unable to connect to the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Recalled by Randox Laboratories Ltd. Due to Randox has now released...
The Issue: Randox has now released further steps to avoid contamination of the Lipase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX DNA MMK Lab Use Recalled by Becton Dickinson & Co. Due to The package...
The Issue: The package insert incorrectly lists the volume of the primer and probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BECKMAN COULTER iChemVELOCITY Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter has determined that there is a potential for incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge AGS Recalled by Getinge Disinfection Ab Due to There is potential...
The Issue: There is potential for a cart with disinfected goods to unload without the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX DNA MMK (SPC) For Laboratory Use Recalled by Becton Dickinson & Co....
The Issue: The package insert incorrectly lists the volume of the primer and probe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU...
The Issue: ICU Medical is expanding the scope of their previously initiated recall to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Smallbore Ext Set w/6-Port NanoClave Manifold Recalled by ICU Medical de...
The Issue: ICU Medical is expanding the scope of their previously initiated recall to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave Manifold Recalled by ICU...
The Issue: ICU Medical is expanding the scope of their previously initiated recall to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.