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. 2,828 recalls have been distributed to Virginia in the last 12 months.
Showing 4821–4840 of 29,425 recalls
Recalled Item: ADVIA Centaur Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VA-LCP Clavicle Plate 2.7 Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RAPIDSORB IPS Battery Pack Recalled by Synthes (USA) Products LLC Due to...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.5MM Drill Bit/QC/85MM Sterile-surgical Recalled by Synthes (USA) Products...
The Issue: Products not sterilized, sterility cannot be confirmed
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM Erythropoietin (EPO) Assay (100 Test) Recalled by Siemens...
The Issue: Siemens Healthcare Diagnostics has confirmed an average negative bias of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Catheter Ext. 6 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Adapter 4 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVS Health Waterproof Wound Tracking Dressing Recalled by MEDLINE...
The Issue: Product failed sterility testing.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Luer Lock Catheter Ext. 18 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stay-safe /Safe Lock Catheter Ext. 12 in Recalled by Fresenius Medical Care...
The Issue: The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component...
The Issue: Invacare Homecare & G-Series Bed Components identified with a potential weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural tray. PERIFIX 17 Ga. x 3-1/2 in. (90 mm) Tuohy Recalled by B. Braun...
The Issue: Kits should contain Filter Straws with Standard Luer Connections however the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head Recalled by...
The Issue: Mislabeled: Packaging incorrectly a MobileLink Dual Mobility insert type F...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Duet External Drainage and Monitoring System Recalled by Medtronic...
The Issue: Potential for catheter disconnection from the patient line stopcock connectors.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.