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. 1,997 recalls have been distributed to Virginia in the last 12 months.
Showing 15081–15100 of 29,425 recalls
Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...
The Issue: The sterility may be compromised due to a potential breach in the packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...
The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...
The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Pear Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard 90 degree Catheter Recalled by PENTAX...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...
The Issue: Philips has discovered through customer complaints and internal testing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...
The Issue: Certain lots are missing a protective sheath component over the silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...
The Issue: Improper design or specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK FT3 (FT3: Free Triiodothyronine) is designed for IN Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...
The Issue: Potential for fluorescein interference to cause inaccurately elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.