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. 2,393 recalls have been distributed to West Virginia in the last 12 months.
Showing 22201–22220 of 27,884 recalls
Recalled Item: 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...
The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....
The Issue: Device software treatment preset parameters for the XC treatment handpiece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...
The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...
The Issue: Customer reports that the ventilator display can freeze. Ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...
The Issue: Customers complained about under-recovery of non-Roche controls and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...
The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...
The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.