The Recall Desk

State

West Virginia product recalls

73,388 recalls have nationwide distribution and so reach West Virginia. 3,571 additional recalls listed West Virginia specifically in their distribution scope.

What the numbers show

Total
3,571
Critical
603
Severe
872
Most recent
2026-10-07

Of the 3,571 recalls naming West Virginia we have scored against our rubric, 603 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 872 (24%) are Severe.

Which agencies issued them

These figures cover only the 3,571 recalls whose distribution notice names West Virginia specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18101–18125 of 76959

  • SevereFDA (Food)·F-0299-2023·2023-01-25

    Greco and Sons Frozen Dough Products Recalled for Undeclared Milk

    Sysco Merchandising and Supply is recalling multiple Greco and Sons frozen dough products because they contain undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 15 FRZN DOUGH 6 oz.; Greco and Sons Dough Room Product No. 16 FRZN DOUGH 8 oz.; Greco and Sons Dough Room Product No. 18 FRZN DOUGH 10 oz.; Greco and Sons Dough Room Product No. 26 FRZN DOUGH 12 oz.; Greco and Sons Dough Room Product No. 19…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0300-2023·2023-01-25

    Greco and Sons dough ball products recalled for undeclared milk allergen

    Sysco is recalling Greco and Sons dough ball products due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 79 North Park Lounge 10 oz.; Greco and Sons Dough Room Product No. 64 North Park Lounge 16 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0297-2023·2023-01-25

    Greco and Sons dough products recalled for undeclared milk allergen

    Sysco Merchandising and Supply recalls Greco and Sons dough products containing undeclared milk allergen. Affected products were distributed to food service locations in six states.

    Product
    Greco and Sons Dough Room Product No. 92 House of 1000 10 oz.; Greco and Sons Dough Room Product No. 81 House of 1000 15 oz.; Greco and Sons Dough Room Product No. 37 Handlebar 27 oz.; Greco and Sons Dough Room Product No. 38 Handlebar 23 oz.; Greco and Sons Dough Room Product…
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V026000·2023-01-25

    2022-2023 BMW i4 and iX Vehicles Lack Pedestrian Warning Sounds

    BMW is recalling 2022-2023 i4 eDrive40 and iX xDrive50 electric vehicles because the external pedestrian warning sound system may fail during start-up. Pedestrians could be unaware of approaching vehicles, increasing injury risk.

    Product
    BMW — BMW IX, I4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0294-2023·2023-01-25

    Sysco Greco and Sons Dough Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons dough products sold in six states due to undeclared milk allergen. The recall affects approximately 2,325 cases with Best if Used By dates between December 1, 2022 and June 1, 2023.

    Product
    Greco and Sons Dough Room Product No. 28 Stefano 12 oz.; Greco and Sons Dough Room Product No. 29 Stefano 20 oz.; Greco and Sons Dough Room Product No. 30 Stefano 26 oz.; Greco and Sons Dough Room Product No. 36 Stefano 24 oz.; Greco and Sons Dough Room Product No. 35 Stefano 15…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0298-2023·2023-01-25

    Sysco Greco and Sons Dough Products Recalled for Undeclared Milk Allergen

    Sysco is recalling Greco and Sons Dough Room products due to undeclared milk allergen. Affected products include 8 oz and 16 oz sizes distributed to six states.

    Product
    Greco and Sons Dough Room Product No. 61 Dad's 8 oz.; Greco and Sons Dough Room Product No. 62 Dad's 16 oz.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0301-2023·2023-01-25

    Dough Ball Products Recalled for Undeclared Milk Allergen

    Sysco Merchandising and Supply is recalling Greco and Sons Dough Room pizza dough products due to undeclared milk allergen. Consumers with milk allergies should not consume these products.

    Product
    Greco and Sons Dough Room Product No. 12 Vic's Pizza 10 oz.; Greco and Sons Dough Room Product No. 17 Vic's Pizza 20 oz.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0978-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains Recalled for Multiple Performance Issues

    Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. No injuries have been reported.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 mm, REF JP-2215
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0987-2023·2023-01-25

    Cardinal Health surgical drain recalled for performance and safety defects

    Cardinal Health is recalling approximately 24,963 Jackson-Pratt Channel Drains due to multiple performance defects including broken tips, dull insertion tools, reduced flexibility, and visibility issues. Units were distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2229
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0968-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains recalled for performance defects

    Cardinal Health is recalling 4,111 Jackson-Pratt Channel Drains (10 Fr) due to multiple performance issues including dull trocars, broken tips, reduced flexibility, and lack of radiopacity that may affect device function.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2187
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0133-2023·2023-01-25

    Drug Recall: Artificial Tears Eye Ointment Due to Manufacturing Deviations

    Akorn, Inc. is recalling Artificial Tears Ointment (1.16 million tubes nationwide) due to manufacturing practice deviations. The firm voluntarily initiated this recall.

    Product
    Artificial Tears OINTMENT, Lubricant Eye Ointment, Net Wt. 3.5 g (1/8 oz.) per tube, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-062-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0139-2023·2023-01-25

    FDA Recalls Nationwide Supply of Erythromycin Ophthalmic Ointment for Manufacturing Deviations

    Akorn, Inc. is recalling 36,455 cartons of Erythromycin Ophthalmic Ointment USP 0.5% nationwide due to manufacturing process deviations. The company voluntarily initiated this Class II recall.

    Product
    Erythromycin Ophthalmic Ointment USP, 0.5%, Net Weight: 1 g per tube (50 unit-dose tubes per carton), Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-070-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0129-2023·2023-01-25

    Local anesthetic Sensorcaine vials recalled for subpotent epinephrine

    Fresenius Kabi is recalling Sensorcaine-MPF local anesthetic vials due to subpotent epinephrine levels. The affected batch (31,600 vials) was distributed nationwide.

    Product
    SENSORCAINE — SENSORCAINE (BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0970-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains Recalled for Multiple Performance Defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance defects including dull trocars, broken tips, and radiopacity issues. 921 units affected worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 15 Fr, REF JP-2189
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0979-2023·2023-01-25

    Cardinal Health Jackson-Pratt Drain Recalled for Multiple Performance Issues

    Cardinal Health is recalling Jackson-Pratt Channel Drains due to multiple performance issues including dull trocars, lack of radiopacity, reduced flexibility, and broken tips. The affected devices were distributed worldwide.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 7 mm, REF JP-2216
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0135-2023·2023-01-25

    Betaxolol ophthalmic solution recalled for manufacturing process violations

    Akorn, Inc. is voluntarily recalling Betaxolol ophthalmic solution (6,273 bottles, lot 1A08A, exp. 12/31/2022) due to manufacturing deviations. Consumers should consult their healthcare provider.

    Product
    Betaxolol Ophthalmic Solution, USP 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-705-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0967-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains Recalled for Performance Defects

    Cardinal Health is recalling 1,150 Jackson-Pratt Channel Drains due to multiple performance defects including lack of radiopacity, dull trocars, reduced flexibility, and broken tips affecting post-surgical wound drainage.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2186
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2023·2023-01-25

    Cardinal Health Jackson-Pratt Wound Drain Recall Due to Performance Defects

    Cardinal Health is recalling Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. The worldwide recall affects units used in post-operative wound drainage.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 28 Fr, REF JP-2290
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0132-2023·2023-01-25

    FDA Recalls Akorn AK-POLY-BAC Eye Ointment for CGMP Violations

    Akorn Inc. voluntarily recalls 36,025 tubes of AK-POLY-BAC Bacitracin/Polymixin B eye ointment nationwide due to manufacturing process deviations affecting product quality and sterility.

    Product
    AK-POLY-BAC brand of Bacitracin cand Polymixin B Sulfate Ophthalmic Ointment USP, 3.5 g (1/8 oz.) tube, Rx only, Sterile, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-238-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0128-2023·2023-01-25

    Prescription Anesthetic Drug Recalled for Subpotent Epinephrine Content

    Fresenius Kabi is recalling Sensorcaine anesthetic injections nationwide due to subpotent epinephrine content. Affected batches may not provide adequate anesthesia or hemostasis during procedures.

    Product
    SENSORCAINE — SENSORCAINE (BUPIVACAINE HYDROCHLORIDE AND EPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0956-2023·2023-01-25

    ARTIS medical imaging systems recalled for mechanical connection failure

    Siemens ARTIS pheno and ARTIS icono imaging systems are recalled because the mechanical connection between the tabletop and table base may fail. The recall affects 550 units distributed worldwide.

    Product
    ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V028000·2023-01-25

    2022 Hyundai Santa Fe Plug-In Hybrid fuel tank defect recall

    Hyundai is recalling certain 2022 Santa Fe Plug-In Hybrid vehicles due to improperly molded fuel tanks that may leak gasoline. A fuel leak in the presence of an ignition source can increase the risk of fire.

    Product
    HYUNDAI — HYUNDAI SANTA FE PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0998-2023·2023-01-25

    FDA Recalls Thoracic Stent-Graft Systems Over Manufacturing Size Defect

    Bolton Medical has recalled 640 units of RELAY PRO thoracic stent-graft systems worldwide because the products may be shorter than their packaging indicates.

    Product
    RELAY PRO, THORACIC STENT-GRAFT SYSTEM, REF 28-N4-XX-XXX-XXX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0984-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains recalled for multiple performance defects

    Cardinal Health is recalling 2,277 Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. These defects may affect the drain's function and clinical performance.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2226
    Category
    Medical Device
    Distribution
    Distributed nationwide