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 21121–21140 of 27,884 recalls
Recalled Item: rainbow Reusable Sensors. RAINBOW DCI-DC3 Recalled by Masimo Corporation Due...
The Issue: These sensors were manufactured with incompatible configurations. This could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DA-2006P - Defibrillator / Pacer Analyzer Recalled by BC Group International...
The Issue: Device is not functioning as intended: Two wires running to the ECG...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Perfusion Tubing Packs Recalled by Medtronic Perfusion Systems Due...
The Issue: This recall is being initiated due to a potential breach of the Tubing Pack...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 5.5: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IOL Master 500: Software versions 7.5 and 7.7 Recalled by Carl Zeiss Meditec...
The Issue: IOL Master software versions 7.5 and 7.7 calculation printouts and exported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN Injectable Implant 1.0 cc Gel Recalled by Merz North America, Inc....
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiesse (+) Lidocaine Injectable Implant 1.5cc Recalled by Merz North...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cavity 8 Gauge Spine Wand indicated for resection Recalled by ArthroCare...
The Issue: There is cracking in the tray when the device is snapped into place. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROLARYN PLUS Injectable Implant 1.0 cc Plus Calcium Hydroxlyapatite (CaHA)...
The Issue: The expiration date encoded in the UDI barcode on the label on the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon GranuFlo Dissolution Unit - P/N G047-80101. For...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Modified Mixer Motor (for 132 Gallon Dissolution Units) Recalled...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 132 Gallon Dry Acid Dissolution Unit Recalled by Fresenius Medical...
The Issue: Dissolution units and replacement motors units do not provide full thermal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amphirion Deep OTW PTA Balloon Catheter: Model numbers: US: AMP015020152...
The Issue: Medtronic has discovered that select lots of the Amphirion Deep PTA Balloon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iOS Galileo Application Version 1.1.1 or lower that programs the Recalled by...
The Issue: A software issue can make the foot move into dorsiflexion, unnoticed by the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential issue with routine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The...
The Issue: Incorrect use of T-Piece resuscitators will result in complete occlusion of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE VC150 Vital Signs Monitor Monitor vital signs in humans Recalled...
The Issue: Monitor may shut down unintentionally without restarting.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Infiniti Plus Needle Guide Recalled by Civco Medical Instruments Co....
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIVCO Biopsy Starter Kit Recalled by Civco Medical Instruments Co. Inc. Due...
The Issue: Sterility of the product cannot be assured.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Single Lumen Embolectomy Catheter 5F Recalled by LeMaitre Vascular,...
The Issue: Manufacturing issue that could cause a pinhole in the formed end of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.