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. 1,047 recalls have been distributed to Virginia in the last 12 months.
Showing 18061–18080 of 53,829 recalls
Recalled Item: BD Phoenix PMIC/ID-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Ares Antibiotic-Impregnated Catheter Recalled by Medtronic...
The Issue: There is a potential for a defect on the seal of the outer pouch of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix" PMIC-109: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-108: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-107: IVD is intended for the in vitro Recalled by Becton...
The Issue: BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization...
The Issue: System table may tilt because the bolts that fasten the vertical column and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system Recalled by...
The Issue: After the user selects the Lock-in command, the kV and mA values are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** spineX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** SHEEHY BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOLMaster 700 Recalled by Carl Zeiss Meditec AG Due to When using software...
The Issue: When using software 1.90.2.09 or 1.90.8.06 and using modality worklist...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grace Medical *** COX BONE DUST COLLECTOR *** Recalled by Oto Med Inc Due to...
The Issue: During internal Age Testing, holes were found in the sterile Tyvek pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Injection Recalled by Hikma Pharmaceuticals USA Inc. Due to...
The Issue: Failed pH Specifications: Out of Specification pH Test Results were found in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TraZODONE Hydrochloride Tablets USP 100 mg Recalled by AVKARE Inc. Due to...
The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sildenafil Tablets USP 100 mg Recalled by AVKARE Inc. Due to Product mix-up:...
The Issue: Product mix-up: Bottles of sildenafil and trazodone were inadvertently...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.