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.

19826–19850 of 75397

  • SevereFDA (Food)·F-1587-2022·2022-08-24

    Maple Soft Serve Mix Recalled Due to Potential Listeria Contamination

    Kingdom Creamery of Vermont is recalling its 5% Maple Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 5% Maple Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1558-2022·2022-08-24

    Albertsons Ready Meals Crab & Shrimp recalled for undeclared allergens

    Albertsons ready-to-eat meals may contain undeclared fish, shellfish, egg, wheat, and soy allergens. Consumers with allergies should not consume and should return the product.

    Product
    Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 OZ CAL 310 NET WT. 0lb 12oz (340g) ready2eat UPC 23253500000 Store Banners: ACME, Albertsons, Andronico s Community Markets, Balducci s, Carrs-Safeway, Eagle, Jewel-Osco, King s, Pak N Save, Safeway, Shaw s, Star Market, Vons
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-1594-2022·2022-08-24

    14% Chocolate Base Mix recalled for potential Listeria monocytogenes contamination

    Kingdom Creamery of Vermont is recalling 1,623 cases of 14% Chocolate Base Mix (Lot 220724, Best By Date 8/11/22) distributed in VT, ME, and MA due to potential Listeria monocytogenes contamination.

    Product
    14% Chocolate Base Mix; Kingdom Creamery of Vermont
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1589-2022·2022-08-24

    Kingdom Creamery of Vermont Maple Soft Serve Mix Recalled for Listeria

    Kingdom Creamery of Vermont's 10% Maple Soft Serve Mix is being recalled due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 10% Maple Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1599-2022·2022-08-24

    Ice cream base mix recalled due to listeria monocytogenes contamination

    SOCO Creamery ice cream base mix is being recalled due to potential Listeria monocytogenes contamination. Affected consumers in Vermont, Maine, and Massachusetts should discard the product.

    Product
    SOCO Creamery 15% Base Mix; the label also lists Kingdom Creamery of Vermont
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1512-2022·2022-08-24

    HeartWare HVAD System Batteries Recalled for Critical Electrical Faults

    HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.

    Product
    HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1597-2022·2022-08-24

    Rococo Ice Cream Base Mix Recalled Due to Listeria Contamination Risk

    Kingdom Creamery of Vermont LLC is recalling Rococo Ice Cream 15% base mix due to potential Listeria monocytogenes contamination. The recalled product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Rococo Ice Cream 15% base mix; list Kingdom Creamery of Vermont on the product label
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1556-2022·2022-08-24

    Albertsons Ready Meals Shrimp recalled for undeclared fish and shellfish allergens

    Albertsons Companies recalled Ready Meals Shrimp Cooked with Cocktail Sauce for undeclared fish and shellfish allergens. The product was distributed across 24 US states.

    Product
    Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste, water, high fructose corn syrup, distilled vinegar, horseradish, salt, lemon juice concentrate, soybean oil, beet powder, natural and artificial flavor…
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-1592-2022·2022-08-24

    Vermont creamery recalls ice cream base mix due to Listeria contamination

    Kingdom Creamery of Vermont is recalling 14% Base Mix and Archie Case Mix ice cream base products due to Listeria monocytogenes contamination. A Class I FDA recall affects 1,623 cases distributed to Vermont, Maine, and Massachusetts.

    Product
    14% Base Mix Case:14% Archie Case Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1586-2022·2022-08-24

    FDA Recalls Kingdom Creamery Vanilla Soft Serve Mix for Listeria Risk

    Kingdom Creamery of Vermont is recalling 5% Vanilla Soft Serve Mix due to potential Listeria monocytogenes contamination. The affected product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Kingdom Creamery of Vermont 5% Vanilla Soft Serve Mix
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-1595-2022·2022-08-24

    Lake Champlain Chocolates 14% base mix recalled for Listeria monocytogenes

    Kingdom Creamery of Vermont LLC is recalling Lake Champlain Chocolates 14% base mix due to potential Listeria monocytogenes contamination. The product was distributed in Vermont, Maine, and Massachusetts.

    Product
    Lake Champlain Chocolates 14% base mix
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1532-2022·2022-08-24

    CURAD First Aid Kit Recalls Due to Improper Storage Temperature

    Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.

    Product
    CURAD FIRST AID KIT, SKU 999037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1524-2022·2022-08-24

    ARIES SARS-CoV-2 Assay may produce false negative diagnostic results

    Luminex Corporation recalled 257 units of the ARIES SARS-CoV-2 Assay (lot AB4042A) due to potential false negative results. The assay may fail to detect the ORF1ab gene, risking missed COVID-19 infections.

    Product
    ARIES SARS-CoV-2 Assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1345-2022·2022-08-24

    IV Trisodium Citrate Solution Recalled for Potential Cross-Contamination Risk

    Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.

    Product
    Trisodium Citrate 0.5% Solution, (0.5%/4L), contains Per Liter: Sodium 140 mmol/L, Chloride 86 mmol/L, Citrate 18 mmol/L, 4000 mL IV bag, packaged in 1 x 1 IV bag per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1543-2022·2022-08-24

    GS Saline Solution recalled due to improper temperature storage

    GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.

    Product
    GS SALINE SOLUTION 12FL OZ, SKU 902274
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2022·2022-08-24

    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT Recalled Due to Improper Temperature Storage

    Family Dollar is recalling LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT that were stored without proper temperature control. Customers should discontinue use of product purchased between May 1 and June 10, 2022.

    Product
    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT, SKU 900265
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1545-2022·2022-08-24

    Simply Saline Nasal Mist Recalled for Improper Storage Conditions

    Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.

    Product
    SIMPLY SALINE NASAL MIST 3.1 OZ, SKU 999801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2022·2022-08-24

    Sterile Surgical Pads and Wound Care Kits Recalled Due to Structural Failure

    ASO LLC is recalling 274,458 retail packages of three wound care products that fall apart during handling after removal from packaging, compromising their sterility and usability.

    Product
    (1) CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads 5 in. x 9 in. per box, ASO Item No. 781083, SKU 894111 (2) CVS Health 30 Piece Wound Care Kit, For Large Size Wounds, ASO Item No. 781240, SKU 998842; and (3) equate First Aid Kit, 120 Items…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1526-2022·2022-08-24

    Pregnancy Test Units Recalled Due to Improper Temperature Storage

    Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.

    Product
    CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU-ID 900260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1344-2022·2022-08-24

    FDA Recalls Neostigmine Methylsulfate Injectable Due to Contamination Risk

    Nephron Sterile Compounding Center is recalling one lot of Neostigmine Methylsulfate Injection due to potential cross-contamination from product carryover during manufacturing. The recall affects 13,500 vials distributed nationwide.

    Product
    PF-Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL (1 mg/mL), One 3 mL Unit-Dose Vial, packaged in 30 x 3 mL Sterile Unit-Dose Vials per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC 69374-932-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1551-2022·2022-08-24

    Dressing Change Kit Recalled for Latex Mislabeling Risk

    Trinity Sterile is recalling Wolf Pak Premium Dressing Change Kits labeled as latex-free. The Non-Adherent Dressing component contains natural rubber latex, creating risk for patients with latex allergies.

    Product
    Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Cs/30 Ref: DC5090LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1549-2022·2022-08-24

    Medical Dressing Kit Recalled for Mislabeled Latex Content

    Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.

    Product
    Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Ref: DC5030LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1555-2022·2022-08-24

    BD PhaSeal Y-Site Connector recalled for mislabeled expiration dates

    Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.

    Product
    BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1348-2022·2022-08-24

    Acetaminophen Injection Recalled for Temperature Storage Abuse Nationwide

    Baxter Healthcare recalls 85,680 bags of acetaminophen injection nationwide due to temperature abuse in distribution. Product was shipped in refrigerated trucks despite being labeled for room temperature storage.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide