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. 1,103 recalls have been distributed to Virginia in the last 12 months.
Showing 12461–12480 of 53,829 recalls
Recalled Item: Aloha Organic Protein Drink Recalled by Lyons Magnus, Inc Due to Findings...
The Issue: Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Aloha Organic Protein Drink Recalled by Lyons Magnus, Inc Due to Findings...
The Issue: Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medline CHEST TUBE REORDER NO: DYNJ36762A Recalled by Medline Industries...
The Issue: Due to a non-sterile component (tape) being place within the sterile portion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TANDEM LIFE LivaNova LIFESPARC Controller Recalled by Cardiac Assist, Inc...
The Issue: Critical Failure of the LifeSPARC controller when the software freezes or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Servo-air Ventilator System-The Servo-air Ventilator System is: Intended for...
The Issue: Device does not meet regulatory requirements of stability while stationary,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications: below specification limits for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Matzim LA (Diltiazem Hydrochloride) Extended-Release Tablets Recalled by...
The Issue: Failed Dissolution Specifications: below specification limits for dissolution.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUSTANGO (Pendenadril Tytrate Blend) Capsules Recalled by Ultra Supplement...
The Issue: Marketed Without an Approved NDA/ANDA: Analytical testing showed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamotrigine Tablets Recalled by AVKARE Inc. Due to Labeling: Label Error on...
The Issue: Labeling: Label Error on Declared Strength
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iSED Primary Pump Tubing Spare Part Kit- (IVD) tubing is Recalled by Alcor...
The Issue: Primary Pump Tubing Spare Part is incorrect. If the tubing is installed onto...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet Critical Care AB/Getinge Servo-u Ventilator System Recalled by...
The Issue: Ventilators may generate a combination of alarms which may result in loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Bronchovideoscope Recalled by Aizu Olympus Co., Ltd. Due to...
The Issue: The recalled unit was utilized in a veterinary endoscopy procedure in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NUCLISENS easyMAG Magnetic Silica Recalled by bioMerieux, Inc. Due to There...
The Issue: There is a potential of no result leading to possible delayed result due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWAS-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner UniGlide Hydrophilic Wire Guide PART NUMBER (RPN): HPWA-35-80...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System with Version 3.7.2 and below Recalled by...
The Issue: Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power electronic box Recalled by Myolyn Inc. Due to Screws mounting an...
The Issue: Screws mounting an internal power supply may come loose during shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NuVasive MD Pulse III Multimodality System Pulse Software Recalled by...
The Issue: Due to an incorrect security key, customers were unable to connect to remote...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner PC Hydrophilic Wire Guide PART NUMBER (RPN): RFSPC-35-180...
The Issue: Product did not meet the acceptance criteria for packaging testing, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.