The Recall Desk

Hazard

Mis Labeling recalls

9,606 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,606
Critical
160
Severe
588
Most recent
2026-09-09

Of the 9,606 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (6%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all mis labeling recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1176–1200 of 9606

  • HighFDA (Devices)·Z-0729-2022·2022-03-16

    Vascular Graft Mislabeled; Packaging Labels Do Not Match Product Specifications

    A vascular graft has been recalled due to labeling mismatch: the outer package label differs from the inner sterile packaging in graft type and dimensions. Implanting the wrong size could disrupt blood vessel connections and create a pseudo-aneurysm.

    Product
    HEMASHIELD GOLD KNITTED MICROVEL DOUBLE VELOUR VASCULAR GRAFT- D: 7 mm; L: 60 cm Indicated for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease. Product Code/REF Number: M002020952070
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0854-2022·2022-03-16

    Coca-Cola Cherry Zero Sugar Recalls Cans Missing PKU Warning Label

    Coca-Cola Cherry Zero Sugar 12-packs distributed in AZ, UT, and WY are being recalled because individual cans lack required phenylketonuric (PKU) warning labels, which are necessary for people with phenylketonuria.

    Product
    Coca-Cola Cherry Zero Sugar Fridge Pack, 12 - 12 FL OZ CANS (144 FL OZ) in a 12-pack fridge pack carton. UPC 049000047516; UPC Cherry Coca-Cola Zero Sugar can 049000047561; Cherry Coca-Cola can 04905004. There are 2 12-packs per case.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0741-2022·2022-03-16

    FISH Diagnostic Probe Kit Color Labeling Error Affects Test Results

    Cytocell Ltd. is recalling a Del(5q) Deletion FISH Probe Kit due to incorrect color labeling on probe components. The mislabeling may cause misinterpretation of test results for patients with AML or MDS.

    Product
    Del(5q) Deletion FISH Probe Kit: In-Vitro Diagnostic to detect deletions in chromosome location from patients with AML or MDS Catalog Number: USA-LPH024
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0829-2022·2022-03-16

    Factor 75 Chili Meal Recalled for Undeclared Milk Allergen

    Factor 75 Fiery Beef & Black Bean Chili meals are being recalled due to undeclared milk allergen. The product was distributed nationwide and may affect consumers with milk allergies.

    Product
    Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-0731-2022·2022-03-16

    Celltrion DiaTrust COVID-19 Rapid Test Kits Recalled for Incorrect Expiration Dates

    Celltrion USA Inc. is recalling 1.2 million DiaTrust COVID-19 rapid test kits due to incorrect expiration dates on packaging. The kits were distributed to 11 states.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    11 states
  • SevereFDA (Devices)·Z-0680-2022·2022-03-09

    Celltrion DiaTrust COVID-19 Rapid Test Kits Recalled for Unauthorized Clinical Use

    Celltrion USA recalled COVID-19 rapid test kits (DiaTrust) in a Class I action. The kits are labeled for research use only, but the firm assured distributors they could be used for clinical diagnosis, which is not authorized.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0685-2022·2022-03-09

    BioPro Titanium Toe Implant Recalled for Incorrect MRI Safety Claims

    BioPro Titanium MPJ toe implants contain incorrect documentation falsely claiming they are MR Conditional without proper testing. Patients should not assume these implants are safe for MRI.

    Product
    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0803-2022·2022-03-09

    Ice Cream Mislabeled: Black Walnut Packed in Cookie Dough Container

    Signature Select Black Walnut Ice Cream was incorrectly packaged in containers labeled as Cookie Dough, which do not declare nuts as an allergen. The product lid correctly identifies the actual flavor.

    Product
    Signature Select Cookie Dough Ice Cream Vanilla Flavored ice cream with chocolate flavored chips and chunks of chocolaty chip cookie dough. Artificial Flavor added. 1.5 qt. paper container. 6 retail units per case. UPC 2113008803 Some container were filled with Black Wal
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0691-2022·2022-03-09

    Titanium MPJ Toe Implant Recalled for Incorrect MR Safety Labeling

    BioPro is recalling Titanium MPJ toe implants (Lot 125651) with inaccurate labeling claiming MR compatibility when the implant has not been tested for magnetic resonance safety. Patients should consult their physician before MRI.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0711-2022·2022-03-09

    Bronchial Microbiology Brush Labeling Error—Cleared Only for Gastrointestinal Use

    Hobbs Medical is recalling 38,357 Bronchial Microbiology Brushes due to labeling that incorrectly indicates bronchial use. The device is cleared only for gastrointestinal use.

    Product
    Bronchial Microbiology Brush, Catalog Number 4310 and 4320. Microbial sampling is performed by compressing a spring as the base of brush wire to expose the brush, scraping the desired surface, and releasing the compression on the spring which retracts the brush back into the shea
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0804-2022·2022-03-09

    Carrot Cake Soft Bake Cookies Recalled for Undeclared Pecan Allergen

    J & M Foods is recalling Favorite Day Carrot Cake Soft Bake Cookies because pecans are listed as an ingredient but not declared in the allergen warning statement, posing a risk to consumers with pecan allergies.

    Product
    Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6 units per case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-0686-2022·2022-03-09

    Titanium Toe Implants Recalled for Incorrect MRI Safety Labeling

    BioPro Titanium MPJ toe implants are recalled because labeling incorrectly claims MRI safety without actual testing. Patients should consult their physician before undergoing MRI procedures.

    Product
    Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0688-2022·2022-03-09

    Titanium Toe Joint Implant Contains False MR Compatibility Claims

    BioPro recalled titanium toe implants due to incorrect claims in documentation about magnetic resonance (MR) compatibility testing that was never conducted. The FDA issued a Class II recall to address the misleading safety information.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0690-2022·2022-03-09

    Titanium Toe Implant Recalled for Incorrect MRI Safety Statements

    BioPro is recalling Titanium MPJ toe implants due to false claims of MRI compatibility. The device instruction manual states it is MRI-safe despite not being tested.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0689-2022·2022-03-09

    Titanium Toe Joint Implant Labeling Error: Unvalidated MRI Safety Claims

    BioPro Titanium MPJ toe implants are recalled due to false documentation claiming MRI safety testing that was never performed. Patients should not undergo MRI with this implant until properly evaluated.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0683-2022·2022-03-09

    BioPro Titanium MPJ Toe Implant Recalled for Incorrect MR Compatibility Labeling

    BioPro is recalling Titanium MPJ toe implants because instructions and patient cards falsely claim the devices are compatible with MRI imaging, when safety testing for this titanium version has not been conducted.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0797-2022·2022-03-02

    Dunkin Caramel Swirl recalled for undeclared milk allergen from mislabeling

    Lyons Magnus is recalling 1900 cases of Dunkin Caramel Swirl because individual containers are incorrectly labeled as Mocha Swirl without allergen warnings but contain milk.

    Product
    Dunkin Caramel Swirl: 6x 64 fl. oz. per case. Product number 4862 UPC case: 10045796048628 Ingredients: Sweetened condensed nonfat milk, high fructose corn syrup, sugar water, brown sugar, caramel color, natural flavors, potassium sorbate (a Preservative), salt. Allergens:
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0660-2022·2022-03-02

    Optima Coil System Recalled for Labeling and Packaging Mix-Up

    BALT USA recalls Optima Coil System embolization devices due to labeling/pouch mix-up that could result in incorrect device selection during surgical procedures. Potential harms include vessel damage and aneurysm rupture.

    Product
    The Optima Coil System consists of an implantable embolization coil comprised of a platinum-tungsten alloy attached to a proximal stainless steel hypo-tube and distal body coil delivery pusher with a radiopaque distal positioning marker and proximal fluorosafe marker. The Optima
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0647-2022·2022-03-02

    Premium Nature Instant Hand Sanitizer Recalled for Subpotent Ethanol

    AMS Packaging Inc is recalling Premium Nature Instant Hand Sanitizer (70% ethyl alcohol) in 8 oz and 16 oz bottles because some bottles contain less ethanol than labeled, reducing effectiveness.

    Product
    Premium Nature Instant Hand Sanitizer, (ethyl alcohol 70%), plastic bottle packaged as (a) 8 OZ, UPC 8 19192 02866 8; (b) 16 OZ, UPC 8 19192 02874 3; Premium Nature, South Plainfield, NJ.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0652-2022·2022-02-23

    Exeter V40 Cemented Hip Stem Labels May Mismatch Between Sizes

    The FDA has recalled Exeter V40 Cemented Hip (150mm) Stems due to a potential labeling mix-up with the 125mm version. Patients who received the device should verify with their surgeon that the correct size was implanted.

    Product
    Exeter V40 Cemented Hip (150mm) Stem, Part Number 0580-1-440
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-0734-2022·2022-02-23

    Organic Roasted Salted Cashews Recalled for Mislabeled Hazelnuts

    Honey Heaven Wholesale Inc is recalling Organic Roasted Salted Cashews because the product contains hazelnuts but is labeled as cashews. Hazelnuts are visible through the package window.

    Product
    Organic Roasted Salted Cashews, Net Weight of 6 oz (170g), UPC 6 16316 76283 1. Product is packed in a brown kraft stand-up paper pouch with plastic front viewing window with a zip-lock top that was heat sealed to close. The labeled cashew package has the ingredient statement
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0642-2022·2022-02-23

    Dental Resin Product Recalled Due to Non-Registered Manufacturing and Mislabeling

    Envisiontec US Llc recalls FLEXCERA BASE dental resin (574 units manufactured April–September 2021) due to manufacturing in a non-FDA-registered facility and mislabeling of country of origin.

    Product
    FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V102000·2022-02-23

    Audi Recalls 2022 RS 5 Models for Incorrect Tire Loading Label

    Audi is recalling 2022 RS 5 vehicles because the B-pillar tire and loading label displays an incorrect maximum weight, which may lead to vehicle overload.

    Product
    AUDI — AUDI RS 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0641-2022·2022-02-23

    Microbiology quality control kit recalled for incorrect inner label

    A KWIK-STIK quality control kit has an incorrect inner label. The product contains Campylobacter coli, but the inner label states Haemophilus influenzae.

    Product
    KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
    Category
    Medical Device
    Distribution
    Distributed nationwide