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. 1,932 recalls have been distributed to Virginia in the last 12 months.
Showing 23621–23640 of 29,425 recalls
Recalled Item: LP Rotate Foot System prosthetic device for fitting lower extremity Recalled...
The Issue: The threads of the outer tube of the shock module of LP Rotate are too...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS inserts Recalled by DePuy Orthopaedics, Inc. Due to The LCS...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...
The Issue: An issue with photon dose calculation for DMLC (Dynamic MLC) plans for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LCS COMPLETE RPS Femoral Implants Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The LCS COMPLETE RPS Knee System has higher rates of revision in Australia...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Correction due to a fault that causes distal SUJ (DSUJ) failures that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FLOW-i Anesthesia System Axillary O2 and Suction Module Recalled by...
The Issue: Maquet has identified that in some FLOW-i Anesthesia System Auxiliary O2 and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steriseal-Cannula Ophthalmic Recalled by Hill-Rom, Inc. Due to The metal...
The Issue: The metal cannula attached to the handpiece can rotate and become dislodged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volk 25D Large Clear BIO Lens with case Recalled by Volk Optical Inc Due to...
The Issue: Mislabeling. The incorrect lot number was engraved on the anodized aluminum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lombart 90D Clear with case Visualization during diagnosis and laser...
The Issue: Mislabeling. The incorrect lot number was engraved on the anodized aluminum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kinemax Stem Extenders Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker received four customer complaints reporting that inside the box...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitagel Recalled by Orthovita, Inc., dBA Stryker Orthobiologics. Due to...
The Issue: Several shipments of Vitagel product (a surgical hemostat) required to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled...
The Issue: During an internal inspection of the production process the firm discovered...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziploop Button Product Usage: The Ziploop Button is a non-resorbable...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ToggleLoc Recalled by Biomet, Inc. Due to The firm is recalling ToggleLocs...
The Issue: The firm is recalling ToggleLocs and Ziploops manufactured in May and July...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LIS27T - Lacrimal Intubation Set RX Only Sterile Used in Recalled by Quest...
The Issue: Expiration date incorrectly printed in Manufacturing Date field on both...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASSO NAV Duo Loop eco Catheters Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the LASSO NAV Duo Loop eco Catheters because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Hydrogel Gauze Dressing 2 x 2 Recalled by Amerx Health Care Corp....
The Issue: Nonapproved labeling claims (Sterile)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 130 Degree Aiming Arm and 125 Degree Aiming Arm Recalled by Synthes,...
The Issue: The guide sleeve has the potential to jam in the Aiming Arms, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.