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 the agency’s own highest classification or reported deaths or serious injuries, 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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24751–24775 of 90113

  • HighFDA (Devices)·Z-1274-2022·2022-06-29

    Colonovideoscope Model CF-H180AL recalled due to narrowed viewing angle

    Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.

    Product
    Colonovideoscope Model CF-H180AL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1156-2022·2022-06-29

    Tretinoin Capsules Recalled Nationwide for Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.

    Product
    Tretinoin Capsules, 10 mg, Rx Only, 100 capsules per bottle, Teva Pharmaceuticals USA Inc., North Wales, PA, 19454, NDC 0555-0808-02.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1153-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled for Manufacturing Quality Issues

    Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1154-2022·2022-06-29

    Testosterone Cypionate Injectable Recalled Due to Manufacturing Sterility Deviation

    Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1359-2022·2022-06-29

    Mars Gummy Candies Recalled for Potential Metal Strand Contamination

    Mars Wrigley is recalling specific varieties of SKITTLES, STARBURST, and LIFE SAVERS gummies due to potential presence of thin metal strands embedded in the candy or loose in bags. Consumers should dispose of affected products.

    Product
    LIFE SAVERS" Gummies " Five Flavor " Wild Berries " Sours LIFE SAVERS" Gummies " Five Flavor 7.0oz, 3.22oz " Wild Berries 7.0oz " Sours 7.0oz, 180g LIFE SAVERS" Gummies " Five Flavor Peg Pack " Wild Berries Peg Pack " Sours Peg Pack
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1322-2022·2022-06-29

    Trader Joe's Chopped Salad Recalled Due to Undeclared Peanut Allergen

    Taylor Farms is recalling Trader Joe's BBQ & Black Pepper Toscano Chopped Salad because it contains undeclared peanuts and peanut lime dressing due to an incorrect master pack. The product poses a risk to consumers with peanut allergies.

    Product
    Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk, Soy, Wheat Dist. & Sold Exclusively By: Trader Joe's, Monrovia, CA 91016
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-1357-2022·2022-06-29

    Mars Skittles, Starburst, and Life Savers Gummies Recalled for Metal Contamination

    Mars Wrigley is voluntarily recalling Skittles, Starburst, and Life Savers Gummies due to potential metal strand contamination. The affected products were distributed nationwide.

    Product
    SKITTLES" Gummies " Original " Wild Berry " Sour " Original 5.8oz, 2.93oz, 12oz " Wild Berry - 5.8oz, 2.93oz, 12oz " Sour 5.8oz " Original Peg Pack, Stand up Pouch " Wild Berry Peg Pack, Stand up Pouch " Sour Peg Pack
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1345-2022·2022-06-29

    Ice cream recall for undeclared tree nut allergen

    Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.

    Product
    Red Button Vintage Creamery Canadian Vanilla Ice Cream, 56 ounce tub, UPC 0 77865 01001 7, Distributed by Associated Foods Stores, Salt Lake City, UT, 84119. Store Frozen.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2022·2022-06-29

    FDA Recalls Catheter Drainage Kits With Wrong Needle Size

    Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.

    Product
    REF: PIG1260K, 6Fr, X10, Safe-t-Centesis Catheter drainage Kit, Sterile EO,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1347-2022·2022-06-29

    Kava Glycerite Recalled Due to High Yeast and Mold Contamination

    EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.

    Product
    Wise Woman Herbals Standardized Kava Glycerite, product is liquid and contains 15 mg Kavalactones (from Piper methysticum) and 9 mg Kavalactones (from Piper methysticum) depending on lot. Dosage: 60 drops 1-2 times a day. Product is packaged in Amber Glass Boston Round…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1151-2022·2022-06-29

    Isopropyl Alcohol bottles recalled for defective containers and leakage

    Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.

    Product
    ISOPROPYL ALCOHOL — ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1155-2022·2022-06-29

    Clonazepam Tablets Recalled Due to Manufacturing Defect

    Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.

    Product
    Clonazepam Orally Disintegrating Tablets, USP, 0.125mg, Rx Only, 60 Tablets, Mfd. by: Sun Pharmaceutical Industries Ltd. Mumbai, India, Dist. by: Sun Pharmaceutical Industries In., Cranbury, NJ 08512, NDC 57664-783-68, packaged in bottles.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1280-2022·2022-06-29

    FDA Recalls Metalogix Slotted 90 Tubular Wrench Due to Manufacturing Error

    New Standard Device Inc is recalling 14 Metalogix Slotted 90 Tubular Wrenches (Lot A29618A) due to a manufacturing error that causes the wrench to strip nuts when torqueing. No injuries have been reported.

    Product
    Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-1281-2022·2022-06-29

    BVI Wet-Field Eraser surgical devices shipped with incorrect tip configuration

    Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.

    Product
    BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current Part Number: 221251
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2022·2022-06-29

    Alcon Clareon IOL mislabeled due to manufacturing error

    Alcon is recalling specific lots of Clareon intraocular lenses (IOLs) due to mislabeling caused by improper manufacturing line clearance. The mislabeling resulted from partial product mixing during overlapping manufacturing runs.

    Product
    Alcon Clareon IOL with AutonoMe Delivery System
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-1342-2022·2022-06-29

    Mia's Bakery Banh Xu Dua Cake Recalled for Undeclared Coconut

    Mia's Bakery recalls Banh Xu Dua cake because coconut is not declared on the product label, posing a risk to consumers with coconut allergies.

    Product
    Mia's Bakery Bahn Xu Dua Wt. 7 oz./198.5 gram UPC: 8 50660 00003 8 Ings: Glutinous Rice Flour, Sugar, Mung Bean, Soy Bean Oil, Water, Sesame Oil, Sodium Benzoate, Black Color, FD & C Yellow 5 & 6, Red #4 and Blue #1. Keep refrigerated after opening 1965 Potrero Grande…
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1282-2022·2022-06-29

    INTERGARD Woven Vascular Graft mislabeled with incorrect size specification

    Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.

    Product
    INTERGARD Woven Vascular Graft is a woven polyester graft coated with a bovine collagen. It has an external velour surface and non-velour inner surface. The device is available in straight tubes and bifurcated configurations, as well as hemabridge, aortic arch, thoracic aortic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1283-2022·2022-06-29

    Cardiac device software recalled for inadequate electrical insulation

    CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.

    Product
    CardioTek EP-TRACER Software V2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1358-2022·2022-06-29

    Mars Wrigley Recalls STARBURST Gummies for Potential Metal Contamination

    Mars Wrigley Confectionery is voluntarily recalling specific STARBURST Gummies varieties due to potential presence of thin metal strands embedded in the product or loose in bags.

    Product
    STARBURST" Gummies " Original " Sours " Sour Berries STARBURST" Gummies " Original 3.5oz, 5.8oz " Sours 3.5oz, 5.8oz " Sour Berries 5.8oz STARBURST" Gummies " Original Share size bag, Peg Pack " Sours Share size bag, Peg Pack " Sour Berries Peg Pack
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1275-2022·2022-06-29

    EVIS EXERA II Gastrointestinal Videoscope Recalled for Incorrect Component Fit

    Olympus is recalling 8 EVIS EXERA II gastrointestinal videoscopes (Model GIF-HQ190) because an incorrect rubber component may have been installed during repair. The incorrect part does not meet the device's design specifications.

    Product
    EVIS EXERA II Gastrointestinal Videoscope-indicated for use within the upper digestive tract (including the esophagus, stomach, and duodenum). Model: GIF-HQ190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·020-2022·2022-06-28

    Creminelli Recalls Mini Parmesan Salami Sticks Due to Undeclared Egg Allergen

    Creminelli Fine Meats is recalling approximately 4,207 pounds of mini parmesan salami sticks because the product contains an undeclared egg allergen.

    Product
    Creminelli Operating LLC — Creminelli Fine Meats Recalls Mini Parmesan Salami Stick Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V459000·2022-06-28

    Hyundai Recalls 2017-2018 Ioniq Hybrids for Fire Risk

    Hyundai is recalling 2017-2018 Ioniq Hybrid and Plug-in Hybrid vehicles because a power relay assembly may overheat, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID, IONIQ PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide