Product Recalls in West Virginia
Product recalls affecting West Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to West Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,372 recalls have been distributed to West Virginia in the last 12 months.
Showing 23541–23560 of 27,884 recalls
Recalled Item: ROSA Surgical Device 2.5.8 It is intended to be used Recalled by Zimmer...
The Issue: Software corrections reactivating the cooperative endoscopy mode.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 500 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 300 CTS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP (Base) Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Recalled by DePuy Orthopaedics, Inc. Due to The...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP CTS Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eye-pak 7407 Tray Support Cover Recalled by Alcon Research, Ltd. Due to The...
The Issue: The peel pouches of the Tray Support Covers may be insufficiently sealed so...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 Recalled by Instrumentation Laboratory Co. Due to Potential for...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACL TOP 700 LAS Recalled by Instrumentation Laboratory Co. Due to Potential...
The Issue: Potential for sample misidentification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON S Family Ultrasound Systems at software versions VC25D Recalled by...
The Issue: There is a potential measurement error with the Auto-Stats (auto statistics)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Ventilator (4-840120DIUU-XX) The PB840 Ventilator System...
The Issue: Covidien is conducting a medical device field correction for specific...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECLAIM DISTAL TAPERED Distal Stem Recalled by DePuy Orthopaedics, Inc. Due...
The Issue: The product can be difficult to remove from the Distal Stem both out of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra Anchor XL with one (#2) Ultrabraid Cobraid Suture Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S Double Loaded Suture Product Code: 72203854 Fastener...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument and MicroScan Walkaway-96 plus...
The Issue: Springs contained in the access door hinge assembly on the Walk Away Plus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid Suture (blue/white) Product Recalled...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...
The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.