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 7181–7200 of 29,425 recalls
Recalled Item: 7.5 cm Large Craniotome Attachment Use with XMax¿ Recalled by The Anspach...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Trilogy 200 Ventilator Recalled by Philips Respironics, Inc. Due to...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 cm Adult Craniotome Recalled by The Anspach Effort, Inc. Due to Ball...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿ Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Craniotome Intended for cutting and shaping bone Recalled by The...
The Issue: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 Thyroglobulin (OUS). For in vitro diagnostic use with Recalled...
The Issue: Potential for Functional Sensitivity to not meet Instructions For Use (IFU)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Garbin Ventilator Recalled by Philips Respironics, Inc. Due to The...
The Issue: The replacement silicone sound abatement foam installed into some Trilogy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 7 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 5 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 4 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 6 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 8 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen Option Stemmed Tibial Component Size 3 Recalled by Zimmer, Inc. Due...
The Issue: Zimmer Biomet is conducting a voluntary medical device recall related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbett Surgical Container Recalled by Turbett Surgical, Inc. Due to Pod may...
The Issue: Pod may have weld failures breaching the sterile barrier and result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invisalign Express 10 Invisalign System Comprehensive Recalled by Align...
The Issue: 3D orthodontic planning software has a defect that leads to an issue where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHIP KIT Recalled by Cardiac Assist, Inc Due to A software update (v1.1.5)...
The Issue: A software update (v1.1.5) has been developed to address the issue of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denticator PICK-A-DENT Recalled by Young Dental Manufacturing I, LLC Due to...
The Issue: mislabeled product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning system software. Recalled by...
The Issue: A reconstruction error may occur when using the Catheter Bending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.