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. 1,849 recalls have been distributed to Virginia in the last 12 months.
Showing 36921–36940 of 53,829 recalls
Recalled Item: Succinylcholine Chloride 20 mg/mL Recalled by Pharmakon Pharmaceuticals,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Radionuclide Radiation Therapy System Product The product is a teletherapy...
The Issue: The latches of the frame adapter can be locked even if the locating pins of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional Recalled...
The Issue: The Surgical Table Cushion (HybriGel Pads) could potentially contain staples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The VITROS¿ Chemistry Products Calibrator Kit 31 Recalled by Ortho-Clinical...
The Issue: There is an incorrect value (data/calibration mathematics) on ADDs. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm three-fluted Radiolucent Drill Bit/Needle Point/145 mm Sterile...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.2 mm Three-fluted drill bit Recalled by Synthes (USA) Products LLC Due to...
The Issue: The sterile packaging may be compromised. A protective cap is to be secured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by VistaPharm, Inc. Due to...
The Issue: Defective Container: Excess lidding material accumulation between the seal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Volt Resistance Heated Socks (All sizes) Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Shoulder Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V3: MINI-PACS/F IMG ST/CLASSIC: REF/Catalog # 1036490...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...
The Issue: There are potential issues with results reporting for certain run-based...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beacon Tip Royal Flush Plus High-Flow Catheter Catheter Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FluoroSet Radiographic Tubal Assessment Set Cannula Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shuttle Select Slip-Cath Catheter Recalled by Cook Inc. Due to Increase in...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aprima Access Nonvascular Introducer Set Accessories Recalled by Cook Inc....
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.