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. 1,936 recalls have been distributed to Virginia in the last 12 months.
Showing 21321–21340 of 29,425 recalls
Recalled Item: Fresenius 2008 Series Hemodialysis Delivery Systems: 2008T Recalled by...
The Issue: Added Warning Statement: Fresenius 2008 Series Hemodialysis Machines False...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Schiller PB 1000 Recalled by Merge Healthcare, Inc. Due to If the PDM is...
The Issue: If the PDM is utilized to output a pressure for computing fractional flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient...
The Issue: Panorama Central Station including the work station View Station, View...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helios HL3T and HLT Track Mounted Dental Lights Product Usage: Recalled by...
The Issue: The firm received two customer complaints local Pelton & Crane distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liko Universal SlingBars Universal SlingBar" 350 Recalled by Hill-Rom, Inc....
The Issue: The center bolt of the sling bar, which connects the bar to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syva Emit Methotrexate Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens Healthcare Diagnostics confirmed that Syva Emit Methotrexate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diana Automated Compounding System Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical Inc. has received a report of compounded volumes not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol III Recalled by Roche Diagnostics Operations, Inc. Due to Due to...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estradiol II Elecsys and cobas e analyzers 190 Recalled by Roche Diagnostics...
The Issue: Due to the risk of a recently identified cross reactivity, the Elecsys...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERO MHI-TM2000 Linear Accelerator System --- Common Name: Medical Linear...
The Issue: In rare cases the VERO/MHI-TM2000 Operator Console could set an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spectra-System Dental Implant 2008 system is comprised of dental...
The Issue: Implant Direct Sybron Manufacturing, LLC is recalling GoDirect Implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management...
The Issue: Complaints were received of restricted/inaccurate flow rate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guardian II Hemostasis Valve Recalled by Vascular Solutions, Inc. Due to...
The Issue: Vascular Solutions became aware of a potential problem with the click...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bigger-Better-Bladder With 3/8" ID tubing Recalled by Circulatory Technology...
The Issue: The seal between the balloon and the housing may leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: dynarex Specimen Containers Recalled by Dynarex Corporation Due to Exterior...
The Issue: Exterior carton is mis-labeled as Sterile. Non-sterile, bulk specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.