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. 2,267 recalls have been distributed to West Virginia in the last 12 months.
Showing 44941–44960 of 48,376 recalls
Recalled Item: HbA1c Flex(R) reagent cartridge (K3105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HB1C Flex(R) Reagent Cartridge (DF105A Recalled by Siemens Healthcare...
The Issue: Positive bias on the lots listed compared to alternate methods and a higher...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Adult Manual Resuscitator Recalled by Carefusion 2200 Inc Due to...
The Issue: CareFusion has received four (4) customer reports of a component (oxygen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fisher & Paykel Healthcare ICON CPAP (continuous positive airway pressure)....
The Issue: Fisher and Paykel Healthcare is recalling the ICON CPAP units because there...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) The STERRAD CYCLESURE 24...
The Issue: Advanced Sterilization Products is recalling certain lots of STERRAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamisil AT (terbinafine hydrochloride cream 1% antifungal) Recalled by...
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration date; The Lot and/or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLIMEPIRIDE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: One oversized tablet was found in a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centricity Enterprise Archive is a software product for receiving Recalled...
The Issue: GE Healthcare has become aware of a potential data loss issue associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 25mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 35mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 90 Degree Cannulated Infant Blade Plate 30mm x 5mm x Recalled by...
The Issue: Post Market Surveillance of the 90 degree Cannulated Infant Blade Plate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amoxicillin Capsules USP 500 mg Recalled by Sandoz Incorporated Due to...
The Issue: Presence of Foreign Substance, Sandoz is recalling certain lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zeiss brand OPMI Pentero C Recalled by Carl Zeiss Meditec, Inc. Due to Carl...
The Issue: Carl Zeiss Meditec is conducting a field corrective action for its OPMI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver¿ PTX¿ Drug-Eluting Peripheral Stent - 6 mm X 80mm Recalled by Cook,...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver PTX Drug-Eluting Peripheral Stent Recalled by Cook, Inc. Due to Cook...
The Issue: Cook Medical has received a small number of complaints related to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS D-Dimer Exclusion II Recalled by BioMerieux SA Due to Customer...
The Issue: Customer complaints about not repeatable results below the detection limit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM KIT Recalled by DePuy Spine, Inc. Due to...
The Issue: During injection of cement, the water in the hydraulic pump leaks past the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Recalled by DePuy Spine, Inc. Due to...
The Issue: During injection of cement, the water in the hydraulic pump leaks past the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONFIDENCE SPINAL CEMENT SYSTEM 11CC PLUS KIT Recalled by DePuy Spine, Inc....
The Issue: During injection of cement, the water in the hydraulic pump leaks past the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Constellation Vision System Pneumatic Handpiece. Indicated for both...
The Issue: Alcon is conducting a Medical Device Removal for the Constellation Pneumatic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.