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. 953 recalls have been distributed to Virginia in the last 12 months.
Showing 48261–48280 of 53,829 recalls
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciprofloxacin Tablets Recalled by Mylan Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 1g/20mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ifosfamide Injection 3g/60 mL Recalled by AmeriSource Bergen Due to...
The Issue: Temperature abuse: Certain vials of Ifosfamide IV products were not at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...
The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...
The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PedFuse Bone Probe Recalled by SpineFrontier, Inc. Due to Bone Probes used...
The Issue: Bone Probes used to create a pathway in pedicle bone were manufactured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm...
The Issue: Exactech is recalling the InteGrip Acetabular Augments due to an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Ceiling Mount MS-1F & MC-1F for use with the Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P21x/5-1 MHz transducer Recalled by SonoSite, Inc. Due to FUJIFILM SonoSite...
The Issue: FUJIFILM SonoSite Inc. remove P21x/5-1 Transducer because the firm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.