The Recall Desk

State

Vermont product recalls

73,388 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total
2,009
Critical
209
Severe
531
Most recent
2026-09-23

Of the 2,009 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 531 (26%) are Severe.

These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20101–20125 of 75397

  • SevereFDA (Drugs)·D-1295-2022·2022-07-27

    Artri Ajo King Tablets Recalled Due to Undeclared Diclofenac

    The FDA is recalling Artri Ajo King tablets nationwide after finding they contain undeclared diclofenac, a prescription anti-inflammatory drug. Affected bottles (lot LTARTKNGOMG30220, expiring December 2025) were sold on Amazon.

    Product
    Artri Ajo King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B092P4615M, UPC 7 501031 111190
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1297-2022·2022-07-27

    Artri King Herbal Supplement Tablets Recalled Nationwide for Undeclared Medication

    Amazon is recalling Artri King herbal supplement tablets nationwide due to FDA laboratory findings of undeclared diclofenac, a pharmaceutical medication not listed on the label. The product was marketed without FDA approval.

    Product
    Artri King Reforzado con Ortiga y Omega 3 tablets, 500 mg, 100-count bottle, Hecho en Mexico por: PLANTAS MEDICINALES DE MEXICO , Melchor Ocampo No. 55 Local D, Delegacion Xochimilco. C.P. 16800, Mexico, D.F., ASIN B084KSV12L, UPC 7 501031 111190
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1389-2022·2022-07-27

    GE Healthcare Anesthesia Systems Recalled for Potential Transducer Connection Reversal

    GE Healthcare anesthesia systems may have reversed oxygen and air transducer connections, potentially affecting proper gas delivery. 5,372 devices worldwide are affected.

    Product
    GE Healthcare Aisys CS2 Anesthesia System, Part number 1011-9050-000; and Avance CS2 and Avance CS2 Pro Anesthesia System, Part number 1009-9050-000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V543000·2022-07-27

    Volkswagen Recalls 2016 Audi and Golf Models for Air Bag Defect

    Volkswagen is recalling 1,216 2016 Audi and Volkswagen vehicles because the front passenger air bag may explode or deploy improperly, posing a risk of serious injury or death.

    Product
    AUDI — AUDI, VOLKSWAGEN S3, A3 SPORTBACK E-TRON, GTI, GOLF R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1338-2022·2022-07-27

    Launch Sequence Aphrodisia Capsules recalled for undeclared tadalafil

    Launch Sequence Aphrodisia Capsules contain undeclared tadalafil, making them an unapproved drug. The recall involves 500 4-count tins distributed nationwide in the USA and Canada.

    Product
    Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1336-2022·2022-07-27

    Dietary supplement found to contain undeclared pharmaceutical drug tadalafil

    Launch Sequence Capsules dietary supplement recalled for containing undeclared tadalafil, an FDA-approved pharmaceutical ingredient. The product was marketed without required drug approval.

    Product
    Launch Sequence Capsules, Dietary Supplement, 60- count bottles, ASIN B07TLPWXDS, UPC Code 641378938375.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1481-2022·2022-07-27

    Honey Caramels Recalled for Undeclared Tree Nuts

    Queen Bee Gardens recalls Honey Caramels Strawberry Lemonade due to undeclared tree nuts. The product may contain pecans, almonds, coconut, macadamia nuts, or walnuts, posing a risk to consumers with tree nut allergies.

    Product
    Honey Caramels Strawberry Lemonade. Net wt. 5.87 oz. PLU Code: 788394 12154 8. Ingredients: Honey, butter (pasteurized cream & salt), cream, natural flavors, nonfat dry milk, whey, agar, algin, natural colors, citric acid and lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1341-2022·2022-07-27

    Loud Muscle Science Recalls Unapproved Capsule Product Marketed as Aphrodisia

    Loud Muscle Science is recalling Launch Sequence Aphrodisia Capsules because they were marketed without FDA approval. The product was distributed nationwide in the USA and Canada.

    Product
    Launch Sequence Aphrodisia Capsules, 4-count tins, ASIN B07QB3S2LV, UPC Code 661020846957.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1271-2022·2022-07-27

    Neostigmine Methylsulfate Injection recalled due to sterility assurance failure

    Nephron Sterile Compounding Center is recalling Neostigmine Methylsulfate Injection due to lack of assurance of sterility. The recall affects 10,700 syringes distributed nationwide.

    Product
    Neostigmine Methylsulfate Injection, USP, 4 mg/4 mL (1 mg/mL) syringe, packaged in 5 x 4 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-942-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1469-2022·2022-07-27

    English Toffee Chocolate Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling English Toffee Milk Chocolate and related products containing undeclared tree nuts. Products were sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    English Toffee Milk Chocolate. PLU Code: 788394 10008 6. English Toffee M/C Bites. PLU Code: 788394 10015 4. English Toffee Bites Individual. PLU Code: 788394 10115 1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1453-2022·2022-07-27

    Black Forest Classic Truffle recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Black Forest Classic Truffle chocolates that may contain undeclared tree nuts not listed on the label.

    Product
    Black Forest Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11900 2. Ingredients: Dark chocolate, honey, butter (pasteurized cream & salt), cream, cherries, pecans, almonds, non-fat dry milk, whey, agar, algin, lecithin & natural flavors.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1263-2022·2022-07-27

    Lidocaine HCl Injection Syringes Recalled for Sterility Assurance

    Nephron Sterile Compounding Center recalls Lidocaine HCl Injection 2% syringes distributed nationwide due to lack of assurance of sterility. Affected lots should not be used.

    Product
    Lidocaine HCl Injection, USP 2%, 100 mg/5 mL (20 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-949-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1452-2022·2022-07-27

    Chocolate Truffles Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling All Milk Classic Truffles (1.4 oz) because they may contain undeclared tree nuts, posing a risk to consumers with tree nut allergies.

    Product
    All Milk Classic Truffle. Net Wt. 1.4 oz. PLU Code: 788394 11275 1. Ingredients: Milk chocolate, honey, butter (pasteurized cream & salt), cream, non-fat dry milk, whey, agar, align & lecithin. Note: Typo on website should be algin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2022·2022-07-27

    Hill-Rom Mattress Microclimate Feature Failure Increases Pressure Ulcer Risk

    Certain Hill-Rom PRO+ MRS mattresses may have a Microclimate Management feature failure that increases patient pressure ulcer risk. Affected units were distributed to 25+ U.S. states and Canada.

    Product
    Hill-Rom PRO+ MRS Surface For Versacare With X-Ray mattress, REF P3255A01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1491-2022·2022-07-27

    Honeymoon Patties Mint Bee Patties recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoon Patties Mint Bee Patties because they may contain undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). The product was sold at retail locations in Colorado, New Mexico, Wyoming, and nationwide online.

    Product
    Honeymoon Patties Mint Bee Patties. Net wt. 8 oz. PLU Code: 788394 14896 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1412-2022·2022-07-27

    Hill-Rom PRO+ Mattress Microclimate Management Failure Increases Pressure Ulcer Risk

    Baxter Healthcare is recalling 404 Hill-Rom PRO+ 36" mattresses due to performance degradation in their heat and moisture management feature. This failure increases the risk of pressure ulcer development in patients.

    Product
    Hill-Rom PRO+ 36" MRS Surface mattress, REF P7924A03.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1466-2022·2022-07-27

    QBee Honeycomb Toffee Milk recalled for undeclared tree nuts

    Queen Bee Gardens is recalling QBee Honeycomb Toffee Milk due to undeclared tree nuts. Consumers with tree nut allergies face a potential allergic reaction risk.

    Product
    QBee Honeycomb Toffee Milk. Net wt. 1.5 oz. PLU Code: 788394 10404 6.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1430-2022·2022-07-27

    SIGNA Premier MRI scanner recalled for elevated acoustic noise hazard

    GE Healthcare's SIGNA Premier MRI scanner is being recalled because under rare conditions, the gradient coils can produce elevated acoustic noise that could potentially cause hearing loss with prolonged exposure.

    Product
    SIGNA Premier magnetic resonance scanner, model 5748519.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1480-2022·2022-07-27

    Queen Bee Honey Caramels Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Red Raspberry because the product may contain undeclared tree nuts. The recalled items were distributed to Queen Bee retail stores in Colorado, New Mexico, and Wyoming, and nationwide via internet sales.

    Product
    Honey Caramels Red Raspberry. Net wt. 5.87 oz. PLU Code: 788394 12143 2. Ingredients: Honey, Butter (Pasteurized Cream & Salt), Cream, Freeze dried Raspberries, Grade A Non-Fat Dry Milk, Whey, Natural Flavors, Agar, Algin and Lecithin.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1445-2022·2022-07-27

    Spinal fusion cross connector recalled for insufficient clamping force

    Aesculap is recalling AESCULAP S4 Cervical Cross Connectors used in spinal fusion surgery due to insufficient clamping force that may cause the connectors to loosen or shift on the spinal rods.

    Product
    AESCULAP S4 Cervical Cross Connector, L26mm, S4C CROSS CONNECTOR FIXED 26MM, product code SW114T. Used in spinal fusion surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1437-2022·2022-07-27

    BD Connecta Plus1 360 Infusion Connector: Potential Housing Leakage

    Becton Dickinson is recalling certain BD Connecta Plus1 360 Blue Blend infusion connectors due to potential leakage at the housing stopcock that could interrupt treatment and expose patients to contamination and biohazardous material.

    Product
    BD Connecta" Plus1 360 Blue Blend Catalog No. 394911 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1484-2022·2022-07-27

    Honeymoons Dark Chocolate Almond Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honeymoons Dark Chocolate Almond for undeclared tree nuts including pecans, almonds, coconut, macadamia nuts, and walnuts. The product was distributed to retail locations in Colorado, New Mexico, and Wyoming, and nationwide online.

    Product
    Honeymoons Dark Chocolate Almond. PLU Code: 788394 14792 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1272-2022·2022-07-27

    Neostigmine Methylsulfate Injection Recalled for Lack of Sterility Assurance

    Nephron Sterile Compounding Center is recalling 64,365 syringes of Neostigmine Methylsulfate Injection nationwide due to lack of assurance of sterility. Patients using affected lots should contact their healthcare provider.

    Product
    Neostigmine Methylsulfate Injection, USP, 5 mg/5 mL (1 mg/mL) syringe, packaged in 5 x 5 mL Pre-Filled Syringes per carton, 6 x 5 Syringe Carton per case, Rx Only, Nephron 503B outsourcing facility, 4500 12th St. Extension, West Columbia, SC 29172, NDC: 69374-902-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1475-2022·2022-07-27

    Honey Caramels Recalled for Undeclared Tree Nuts

    Queen Bee Gardens is recalling Honey Caramels Cinna Honey due to potential undeclared tree nuts (pecans, almonds, coconut, macadamia nuts, walnuts). Affected products were sold at 10 retail locations in Colorado, New Mexico, and Wyoming, as well as nationwide via internet.

    Product
    Honey Caramels Cinna Honey. Net wt. 5.87 oz. PLU Code: 788394 12404 4. Ingredients: Honey, butter (pasteurized cream & salt), cream, nonfat dry milk, whey, cinnamon oil, beet juice (color), lecithin, algin & agar.
    Category
    Food
    Distribution
    Distributed nationwide