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. 2,807 recalls have been distributed to Virginia in the last 12 months.
Showing 8261–8280 of 29,425 recalls
Recalled Item: Ivenix Infusion System (IIS) Recalled by Ivenix, Inc. Due to Downstream...
The Issue: Downstream occlusion alarm is sometimes immediately followed by a pump...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper...
The Issue: Part (A-rubber) intended for a different model of gastrointestinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonovideoscope Model CF-H180AL Recalled by Olympus Corporation of the...
The Issue: A (Camera unit) CCD intended for a different model of colonoscope may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Bard Peripheral Vascular Inc Due to There is the potential that...
The Issue: There is the potential that a 6 Fr Catheter Drainage kit contains an 8 Fr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Synergy Washer/Disinfector Recalled by Steris Corporation Due to...
The Issue: The firm identified that when the electrical contactor component in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUR-FIT Natura S4S Durahesive Wafer 70MM (1X10PK) US. Each market Recalled...
The Issue: Firm received 10 complaints of skin barrier delamination issues (e.g. flange...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...
The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version...
The Issue: Due to interference with the Live Listen feature of hearing aid or AirPods,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the...
The Issue: Mismatch between the expiration date on the sterile barrier pouch and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...
The Issue: Product label was printed without the UDI number and warning label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...
The Issue: The warning label was printed with the incorrect weight capacity. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Prong Manifold Set (with Luer Connectors) Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus235- Proton Therapy System: to produce and deliver a proton Recalled...
The Issue: First layer of Uniform Scanning treatment fields is sometimes irradiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The C304-HIS device features a guide wire to access the vein Recalled by...
The Issue: The firm's internal processes identified that certain lots may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System Recalled by...
The Issue: Firm detected an increase in complaints related to fractured jaw tips of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.