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.

Which agencies issued them

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.

1026–1050 of 9606

  • HighFDA (Food)·F-1683-2022·2022-09-07

    Great Value Chopped Walnuts Recalled Due to Pecan Mislabeling

    Great Value Chopped Walnuts pouches containing pecans have been recalled from Walmart distribution centers in North Carolina and Florida. The product was mislabeled, which may affect consumers with nut allergies.

    Product
    Great Value Chopped Walnuts, NET WT 4oz (113g); Ingredients: Walnuts DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716; UPC 0 78742 20134 4
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1681-2022·2022-09-07

    Priyems Mango Pickles recalled for undeclared wheat starch

    Yem Foods LLC is recalling Priyems Mango Pickles (1lb/454g) due to undeclared wheat starch from asafoetida. Consumers with wheat allergies may be at risk.

    Product
    Priyems Mango Pickles 1lb/454g UPC 8 61754 000179, 10 retail units per wholesale case, Refrigerated
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Drugs)·D-1472-2022·2022-09-07

    Nighttime Sleep-Aid tablets recalled due to carton labeling error

    CVS Pharmacy is recalling Nighttime Sleep-Aid tablets because the carton incorrectly identifies the active ingredient as doxylamine succinate HCl instead of doxylamine succinate. Approximately 257,064 cartons were distributed nationwide.

    Product
    Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 34873 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1474-2022·2022-09-07

    Isopropyl Alcohol Product Contains Undeclared Ethyl Alcohol

    Luxury 70% Isopropyl Alcohol distributed in Virginia by TSM Brands LLC contains undeclared ethyl alcohol, creating a mislabeling hazard. Consumers should stop using the product.

    Product
    Luxury 70% Isopropyl Alcohol, 16 FL. OZ. (1 PT) 473 ML, Distributed by: TSM Brands LLC, 540 Equinox Ln, Manalapan, NJ 07726, UPC 868275965734.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1573-2022·2022-08-31

    Mizuho OSI Femoral Hooks Recalled for Incorrect Model Etching

    Mizuho OSI is recalling one batch of regular femoral hooks that were etched with an incorrect model designation. The recalled batch contains 13 devices distributed in the United States and Canada.

    Product
    HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1567-2022·2022-08-31

    Stryker SWANSON Finger Joint Implant Incorrect Sizing Label on Carton

    Wright Medical Technology is recalling 17 Stryker SWANSON Finger Joint Implants (size 00) due to incorrect sizing labels applied to carton packaging. Devices with lot numbers 1728375 and 1728376 were distributed across multiple US states and internationally.

    Product
    Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone, Size: 00, REF 4700020, Sterile.
    Category
    Medical Device
    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 (Food)·F-1544-2022·2022-08-24

    HEB Ice Cream Recalled for Undeclared Wheat Allergen

    HEB Creamy Creations Light Mint Chocolate Chip ice cream (880 cups) is recalled due to undeclared wheat. Consumers with wheat allergies are at risk.

    Product
    HEB Creamy Creations Light 1/1 The Fat 1/3 Fewer Calories Of Regular Ice Cream Mint Chocolate Chip Ice Cream Half Gallon (1.89L) UPC 4122048399 packaged in a paper carton with a paper lid with a plastic edge
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·PHA-08242022-01·2022-08-24

    USDA Alerts on Poultry and Meat Products with Undeclared Milk Allergen

    USDA FSIS issued a public health alert for poultry and meat products containing corn starch with undeclared milk. Consumers should not eat these products.

    Product
    FSIS Issues Public Health Alert for Poultry and Meat Products Containing FDA-Regulated Corn Starch That Has Been Recalled Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1550-2022·2022-08-24

    Dressing Change Kit Mislabeled as Latex-Free Contains Natural Rubber Latex

    Trinity Sterile's Wolf Pak Premium Dressing Change Kit is mislabeled as latex-free but contains natural rubber latex in component 94-7002. This poses a risk to people with latex allergies.

    Product
    Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Ref: DC5040LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2022·2022-08-17

    MetaFix hip stem mislabeled with wrong size and batch information

    A Corin MetaFix hip stem (size 7 collarless) was incorrectly labeled as a size 3 collared stem with wrong batch information. The labeling error creates risk during surgical implantation.

    Product
    Corin METAFIX HIP STEM, SIZE 3, STANDARD, 135 degrees, COLLARED HIP STEM, CEMENTLESS, Part Number 579.0103
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1541-2022·2022-08-17

    Whey Protein Powder Recalled for Undeclared Milk Allergen

    Nature's Sunshine Products is recalling Aivia Whey Protein+ Power Herbs Vanilla Bean due to missing milk allergen declaration on the label. Consumers with milk allergies may be at risk.

    Product
    Aivia Whey Protein+ Power Herbs Vanilla Bean, NET WT. 1.33 LBS (602 G) Manufactured by Nature s Sunshine Products, Inc. 1655 N Main Street Spanish Fork, Utah 84660. UPC 0 99904 22712 5 Label is read in parts: "***INGREDIENTS: Whey Isolate, Whey Concentration***".
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1329-2022·2022-08-17

    Lamotrigine Tablets Recalled for Label Strength Error

    AVKARE Inc. is recalling 8,328 bottles of Lamotrigine Tablets, USP 100 mg nationwide due to a labeling error in the declared strength.

    Product
    LAMOTRIGINE — LAMOTRIGINE (LAMOTRIGINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1508-2022·2022-08-17

    Cholestech LDX cholesterol test cassettes require bilirubin interference label update

    Alere is updating the package insert for Cholestech LDX cholesterol test cassettes to disclose that samples with elevated bilirubin can produce inaccurate triglyceride and HDL results. Approximately 436,990 units are affected.

    Product
    The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL cholesterol, triglycerides and glucose. Samples used for testing can be whole blood from a fingerstick (collected in a lithium heparin-coated capillary tube) or
    Category
    Medical Device
    Distribution
    31 states
  • SevereFDA (Drugs)·D-1333-2022·2022-08-10

    SANGTER Energy Supplement Capsules Recalled for Undisclosed Sildenafil

    Distributor RFR, LLC is recalling SANGTER Energy Supplement Capsules because FDA analysis found they contain undisclosed sildenafil without FDA approval. The product was distributed nationwide and internationally.

    Product
    SANGTER Energy Supplement Capsules, 3000mg x 7 grain, 7-count blister pack within a carton, Distributed by: Distributor RFR, LLC, (800) 519-0204 Miami 33172 FL, USA; UPC 0 705632 523285
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V615000·2022-08-10

    Lexus Recalls RC F Vehicles for Missing Tire Weight Label

    Lexus is recalling 2020-2022 RC F vehicles because the tire information label lacks the vehicle's weight capacity, which may increase crash risk.

    Product
    LEXUS — LEXUS RC F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1492-2022·2022-08-10

    EkoSonic Endovascular Device Kit Mislabeled: Boston Scientific Recall

    Boston Scientific is recalling 10 units of the EkoSonic Kit endovascular device due to product mislabeling. Affected devices were distributed to medical facilities in 10 US states.

    Product
    EkoSonic Kit 106cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC components. They are placed into the respective trays and sealed in a Tyvek pouch. The sealed pouches are placed inside the kit carton (box) and the product la
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-1453-2022·2022-08-03

    NuVasive Simplify Disc UDI Barcode Contains Incorrect Size Information

    NuVasive Simplify Disc cervical implants have UDI barcodes with incorrect Global Trade Item Numbers that may cause selection of the wrong device size during implant surgery.

    Product
    Description/Part: Simplify Disc Size 1, Ht 5/SM-5; Simplify Disc Size 1, Ht 6/SM-6; Simplify Disc Size 2, Ht 4/MD-4; Simplify Disc Size 2, Ht 5/MD-5; Simplify Disc Size 2, Ht 5, 5/MD-5L; Simplify Disc Size 2, Ht 6/MD-6; Simplify Disc Size 2, Ht 6, 5/MD-6L; Simplify Disc
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·F-1502-2022·2022-07-27

    Panera Bread Southwest Corn Chowder Recalled for Undeclared Wheat

    Blount Fine Foods is recalling Panera Bread at Home Southwest Corn Chowder due to undeclared wheat. The product poses a health risk to consumers with wheat allergies or celiac disease.

    Product
    Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g)
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1447-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites recalled for undeclared soy allergen

    Chuckanut Bay Foods is recalling Dipped Cheesecake Bites (Pumpkin) because the product contains undeclared soy lecithin. The label incorrectly lists sunflower lecithin, creating a health risk for consumers with soy allergies.

    Product
    Item 39408-12, Chuckanut Bay DIPPED CHEESECAKE BITES Pumpkin. Perishable - Keep Refrigerated. There are 4 pieces per pack and 12 packs per case. Net wt. 3.2 oz per package. UPC 6 03812 39408 6. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***, PUMPKIN, CANE SUGAR,
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-1485-2022·2022-07-27

    Honeymoons Milk Chocolate Cashew recalled for undeclared tree nuts

    Queen Bee Gardens is recalling Honeymoons Milk Chocolate Cashew candy due to undeclared tree nuts including pecans, almonds, coconut, macadamia, and walnuts. Consumers with tree nut allergies face potential serious health risks.

    Product
    Honeymoons Milk Chocolate Cashew. PLU Code: 788394 14828 6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1436-2022·2022-07-27

    Chuckanut Bay Cheesecake Bites Recalled for Undeclared Soy Lecithin

    Chuckanut Bay Foods is recalling Cheesecake Bites that contain undeclared soy lecithin, listed on the label as sunflower lecithin. Consumers with soy allergies may face serious risk.

    Product
    Item 38180-12, Chuckanut Bay Cheesecake Bites New York + Chocolate. Perishable - Keep Refrigerated. There are 8 pieces per plastic clamshell pack and 12 packs per case. Net wt. per pack 6.4 oz. UPC 6 03812 38180 2. The label is read in parts: "***INGREDIENTS: CREAM CHEESE***,
    Category
    Food
    Distribution
    13 states
  • 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 (Food)·F-1503-2022·2022-07-27

    Chicken Breading Recalled Due to Undeclared Wheat Allergen

    Belmatt Inc is recalling Targil's Hot Tails Louisiana Crawfish House Chicken Breading (5,083 pounds, Lot 0206102202) due to undeclared wheat. The product was distributed in Louisiana and poses a risk to consumers with wheat allergies.

    Product
    Targil's Hot Tails Louisiana Crawfish House Chicken Breading packaged in 25lb boxes
    Category
    Food
    Distribution
    1 state