The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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20476–20500 of 27461

  • HighFDA (Devices)·Z-0283-2023·2022-11-30

    Regard LAMINECTOMY surgical kits recalled due to recalled 3M drapes

    ROi CPS LLC is recalling Regard LAMINECTOMY surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled.

    Product
    regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0288-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Defective 3M Surgical Drapes

    ROi CPS LLC is recalling regard BASIC NEURO surgical convenience kits containing 3M surgical drapes that were previously recalled. Affected units were distributed to LA, MO, NC, and FL.

    Product
    regard BASIC NEURO, NU00259S, Item Number 800021019; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0304-2023·2022-11-30

    Hip Arthroplasty Surgical Convenience Kits Recalled Due to Defective 3M Drapes

    ROi CPS LLC is recalling regard TOTAL HIP ARTHROPLASTY surgical convenience kits containing recalled 3M surgical drapes distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0319-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included 3M Surgical Drapes

    ROi CPS LLC is recalling 54 regard LATERAL SHOULDER surgical convenience kits containing 3M surgical drapes that were subsequently recalled by the manufacturer. Affected kits were distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard LATERAL SHOULDER, OR01044C, Item Number 880435003; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0274-2023·2022-11-30

    Basin Set Medical Device Kit Contents Do Not Match Label

    American Contract Systems, Inc. is recalling a surgical basin set (MEBS42K) because the kit contents do not match the labeled contents. The mismatch could result in improper surgical preparation.

    Product
    BASIN SET, MEBS42K, general surgical kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0166-2023·2022-11-30

    G FUEL Watermelon Limeade Energy Drink recalled for incorrect caffeine labeling

    G FUEL LLC is recalling 48,000 units of GFUEL brand Watermelon Limeade Energy Drink nationwide because the product label does not declare the correct amount of caffeine.

    Product
    GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; ready-to-drink energy beverage in a can
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0292-2023·2022-11-30

    Neurosurgery Kits Recalled Due to Defective 3M Surgical Drapes

    ROi CPS LLC is recalling 38 neurosurgery convenience kits distributed in four states because they contain 3M surgical drapes that were separately recalled.

    Product
    regard CERVICAL PACK, NU00303H, Item Number 800058008; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0300-2023·2022-11-30

    Regard Retinal Pack surgical kits recalled for defective 3M drapes

    ROi CPS LLC is recalling Regard Retinal Pack surgical kits distributed in Louisiana, Missouri, North Carolina, and Florida because they contained recalled 3M surgical drapes.

    Product
    regard RETINAL PACK, EY00935C, Item Number 800730003; EYE surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0285-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included Recalled Surgical Drapes

    ROi CPS LLC is recalling 326 regard TOTAL JOINT surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida. The kits contain 3M surgical drapes that were previously recalled. No illnesses or injuries have been reported.

    Product
    regard TOTAL JOINT, OR00446F, Item Number 880291; orthopedic surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0309-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included 3M Surgical Drapes

    Surgical convenience kits are being recalled because they contained 3M surgical drapes that were subsequently recalled. 177 kits distributed in Louisiana, Missouri, North Carolina, and Florida are affected.

    Product
    regard SHOULDER PACK, GS00125V, Item Number 880120022; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0318-2023·2022-11-30

    Regard Shoulder surgical kits recalled due to defective included drapes

    ROi CPS LLC is recalling Regard SHOULDER surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled. Affected kits were distributed to healthcare facilities in LA, MO, NC, and FL.

    Product
    regard SHOULDER, GS00828G, Item Number 880367007; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·22V882000·2022-11-29

    Travel trailer LP gas fittings may crack and leak, risking fire

    Holiday House is recalling 2021–2022 travel trailers because the quick disconnect fittings in the LP gas system may be cracked, causing gas leaks that could lead to fires. Owners should contact Holiday House for inspection and free replacement.

    Product
    HOLIDAY HOUSE — 2022 HOLIDAY HOUSE 24TB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V884000·2022-11-29

    Winnebago travel trailers recalled for incorrect cargo capacity labels

    Winnebago is recalling certain 2021-2022 Minnie and Voyage travel trailers due to incorrect cargo carrying capacity labels, which could lead to vehicle overloading and loss of control.

    Product
    WINNEBAGO — 2022 WINNEBAGO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0066-2023·2022-11-23

    Hand Sanitizer Recalled for Methanol Contamination — FDA Class I

    Adam's Polishes ALCOHOL BASED HAND SANITIZER (multiple sizes) is recalled nationwide because FDA analysis found methanol contamination. This Class I recall poses a serious chemical health risk.

    Product
    Adam's Polishes ALCOHOL BASED HAND SANITIZER, isopropyl alcohol 75% v/v, packaged in a) 4 fl. oz (118) spray bottle, NDC 74943-125-04; b) 8 fl. oz (237 mL) spray bottle, NDC 74943-125-08; c) 1 PINT / 16 fl. oz (475 ml.) spray bottle, NDC 74943-125-16; and d) 1 GALLON / 128 fl. oz
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V873000·2022-11-23

    2022 Chevrolet Silverado 1500 Air Bag System Defect Recall

    General Motors is recalling 5 2022 Chevrolet Silverado 1500 vehicles due to a manufacturing defect that left the air bag sensing diagnostic module in manufacturing mode. The module was not activated at the assembly plant, meaning air bags will not deploy in a crash.

    Product
    CHEVROLET — 2022 CHEVROLET SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0151-2023·2022-11-23

    Zingerman's Pumpkin Gelato Recalled for Undeclared Egg Allergen

    Zingerman's Creamery is recalling Harvest Pumpkin Gelato due to undeclared egg allergen. The recall affects pints and quarts distributed in Michigan.

    Product
    Zingerman's Harvest Pumpkin Gelato pint (16oz) and quart (32oz) sizes
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0152-2023·2022-11-23

    Zingerman's Paw Paw Gelato recalled for undeclared egg allergen

    Zingerman's Creamery is recalling Paw Paw Gelato in pint (16 oz) and quart (32 oz) sizes due to undeclared egg. Consumers with egg allergies should not consume this product.

    Product
    Zingerman's Paw Paw Gelato pint (16oz) and quart (32oz) sizes
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·22V870000·2022-11-23

    2023 IC Bus Models Suspension and Steering Fastener Recall

    Navistar is recalling 2023 IC Bus EV, CE, and RE models due to improperly heat-treated fasteners in suspension and steering joints. These fasteners may lose tension and cause steering instability, increasing crash risk.

    Product
    IC BUS — 2023 IC BUS EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V865000·2022-11-23

    Jeep Wrangler engine shutdown from loss of communication

    Certain 2021-2023 Jeep Wrangler 4xe vehicles may experience engine shutdown due to communication loss, reducing drive power and increasing crash risk.

    Product
    JEEP — 2023 JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V866000·2022-11-23

    2022 Dodge Charger Transmission Shifter Assembly Defect Recall

    Chrysler is recalling the 2022 Dodge Charger for shifter assembly defects. An improperly heat-treated shifter may slip out of drive position, causing sudden loss of power and increasing crash risk.

    Product
    DODGE — 2022 DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0154-2023·2022-11-23

    Omnipod Dash PDM Insulin Pump Remote Recalled for Battery Fire Hazard

    Insulet Corporation is recalling the Omnipod Dash PDM remote controller for insulin pumps due to battery defects causing overheating, swelling, and fire hazard. A fire incident has been reported.

    Product
    18239: ASM Omnipod Dash PDM, insulin delivery system. PT-000010: Assembly, Dash Final PDM U100, mg/dL PT-000011: Assembly, Dash Final PDM U100, mmol/L PT-000030: Assembly, DASH PDM, Canada Remote Controller (Personal Diabetes Manager or PDM) associated with Insulin Pump (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V869000·2022-11-23

    International and IC Bus vehicles recalled for defective suspension and steering fasteners

    Navistar is recalling certain 2021-2023 International trucks and IC Bus vehicles because hex flange lock nuts in suspension and steering joints were improperly heat treated and may lose tension, creating a risk of steering instability.

    Product
    INTERNATIONAL — 2023 INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0239-2023·2022-11-23

    Operating Table Extension Tabletop May Drop, Creating Patient Fall Hazard

    The back rest of Getinge operating table extension tabletops may drop unexpectedly, posing a fall hazard to patients. No injuries have been reported.

    Product
    Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0163-2023·2022-11-23

    Abbott Similac Stage 1 infant formula recalled for compromised seal integrity

    Abbott Laboratories is recalling Similac Stage 1 infant formula due to compromised seal integrity on 14,588,544 bottles. The defect could allow product spoilage.

    Product
    Similac Stage 1 (Export Colombia) 2 fl oz reclose able plastic bottle Packaged as: 48 count case
    Category
    Food
    Distribution
    1 state