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. 1,943 recalls have been distributed to Virginia in the last 12 months.
Showing 17621–17640 of 29,425 recalls
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Constrained Condylar Offset Screw Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optetrak Offset Tibial Tray and Screws Recalled by Exactech, Inc. Due to...
The Issue: There is a design incompatibility between certain sizes of the offset spine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroPort Orthopedics SCHANZ SCREW SELF DRILL Recalled by MicroPort...
The Issue: The item is being recalled due to an inadequate pouch seal. This defect has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection Tubes for...
The Issue: Increased amount of residual blood present on the top of stopper well after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR PS KNEE(TM) e+ Recalled by Encore Medical, Lp Due to It was reported...
The Issue: It was reported that an implant labeled as 343-13-708 was packaged with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Airway Clearance System Recalled by HILL-ROM MANUFACTURING, INC. Due...
The Issue: Monarch Electromagnetic Interference (EMI) may disrupt the operation of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic 3 Intermittent Catheters- 12 Male - 30 catheters per box Recalled by...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroSil Gripper Intermittent Catheters- 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Personal Intermittent Catheters- 16" and 10" lengths - 30 catheters per box...
The Issue: Several instances of a catheter caught in the sterile barrier seal and in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 14-442000S Antegrade Femoral Nail Instrument Kit Recalled by Zimmer Biomet,...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phoenix Antegrade Femoral Nail Trochanteric and Piriformis fossa Recalled by...
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 979195 Loaner Kit for femoral intramedullary nail. Orthopedic instrument....
The Issue: Fracture of the bolt connecting the insertion guide to the intramedullary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT DE handheld data processing module for clinical use Recalled by...
The Issue: Issues resulting from upgrade to software version 2.8: (1) Location,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60 Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OTTO BOCK Kenevo knee joints Model 3C60=ST Recalled by Otto Bock Healthcare...
The Issue: Otto Bock Healthcare Products GmbH has identified a design issue through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.