The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (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.

8951–8975 of 9622

  • HighFDA (Food)·F-0918-2013·2013-01-30

    Conagra Recalls Andy Capp's Cheddar Cheese Fries Due to Unlabeled Soy

    Conagra Inc is recalling Andy Capp's Cheddar Cheese Fries because they were packaged in Hot Fries bags that do not list soy as an ingredient.

    Product
    Andy Capp's Cheddar Cheese Fries packaged in Andy Capp's Hot Fries, 0.85-oz foil bags, snack size, Case UPC: 20-0-26200-47169-7 and Unit UPC: 00-0-26200-47168-6.
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0717-2013·2013-01-30

    Ansell Recalls Lifestyles Condoms Due to Mislabeling of Ultra Thin Style

    Ansell Healthcare Products LLC is recalling one lot of Lifestyles Pleasure Collection condoms because Ultra Thin condoms were included instead of the labeled Skyn style.

    Product
    Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of Ultra Sensitive, Flavors and Colors, Skyn, Thryll, Thyn, and Ultra Thin. UPC 0-70907-02625-0.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0916-2013·2013-01-30

    Cardinal Health Recalls Dairy Aid Lactase Caplets Due to Labeling Error

    Cardinal Health is recalling specific lots of Dairy Aid Lactase Enzyme Supplement caplets because the packaging incorrectly lists the strength as 9,000 FCC Units instead of 3,000 FCC Units.

    Product
    Dairy Aid Lactase Enzyme Supplement, Caplet, 3,000 FCC Units, 60 caplets, OTC, Repackaged by: Cardinal Health, Zanesville, OH 43701, NDC 55154-1335-4
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0715-2013·2013-01-30

    Medisystems 17 Gauge AV Fistula Needles Recalled for Mislabeling

    Medisystems is recalling 17 Gauge AV Fistula Needles because single needle packs are mislabeled as 15 Gauge. The recall covers 4,000 needles distributed in New York, Pennsylvania, and Tennessee.

    Product
    Medisystems 17 Gauge x 1" inch AV Fistula Needle Product Code: D9-2007MGLB Product Usage: Medisystems AVF with MasterGuard anti-stick needle protector is indicated for use as a vascular access device in hemodialysis or other extracorporeal procedures. It is intended for use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0924-2013·2013-01-30

    Pepsi Wild Cherry Recall Due to Swapped Labels

    Pepsi Cola North America is recalling Regular and Diet Wild Cherry Pepsi two-liter bottles because labels were swapped during production, posing a risk to individuals with phenylketonuria or diabetes.

    Product
    Regular Wild Cherry Pepsi two liter plastic bottles UPC 1231100
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-0716-2013·2013-01-30

    Abbott i-Stat cTnI Cartridges Recalled for Incorrect Barcode

    Abbott Point of Care Canada Limited is recalling 10 boxes of i-Stat cTnI cartridges from lot P12179 due to incorrect barcodes on the cartridge portion pack.

    Product
    Abbott Point of Care i-Stat cTnI cartridge. The i-Stat cardiac troponin I (cTnI) test is an in vitro diagnostic test for the quantitive measurement of cardiac troponin I (cTnI) in whole blood or plasma. Measurements of cardiac troponin I are used in the diagnosis and treatment
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0714-2013·2013-01-30

    Medisystems Buttonhole Needle Set Recalled for Mislabeled Length

    Medisystems is recalling 5 mislabeled buttonhole needle pouches that were labeled as 15 Ga x 1 inch instead of 15 Ga x 3/5 inch.

    Product
    Medisystems 15 Gauge x 3/5 inch Buttonhole Needle Set Product Code: BH-2035PE Product Usage: Medisystems Buttonhole Needle Sets are indicated for use as an access device for dialysis and pheresis procedures using a constant site orbuttonhole method of needle insertion.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0886-2013·2013-01-23

    Woodstock Tamari Almonds Recalled for Undeclared Soy Ingredient

    Woodstock Farms is recalling Tamari Almonds because the label fails to list soy, a major allergen, posing a risk of severe allergic reactions.

    Product
    Woodstock All Natural Tamari Almonds, 7.5 OZ in a gusseted re-sealable poly bag.
    Category
    Food
    Distribution
    26 states
  • SevereFDA (Food)·F-0879-2013·2013-01-23

    Somersault Cinnamon Crunch Recalled for Undeclared Milk Allergen

    Somersault Snack Co. is recalling Cinnamon Crunch sunflower seed snacks because the packaging failed to declare a milk allergen present in a flavor ingredient.

    Product
    Somersault brand Cinnamon Crunch. Crunchy nuggets baked with sunflower seeds and toasted grains. Sunflower seed snack. .5 oz, 1 oz., 2 oz., 6 oz., and 16 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0880-2013·2013-01-23

    Unilever Recalls Knorr Pasta Sides for Potential Soy Contamination

    Unilever is recalling Knorr Pasta Sides Cheesy Bacon Macaroni because some pouches may contain soy due to a packaging error.

    Product
    Knorr Pasta Sides Cheesy Bacon Macaroni Net Wt. 3.8 oz, (107 g) Unilever Englewood Cliffs, NJ 07632 USA Made in Canada from domestic and imported ingredients Case SCC 10041000082488 UPC 4100008248
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0691-2013·2013-01-23

    Quanta System Q-Plus T Laser Recall for Promotional Material Labeling

    Quanta System is recalling 75 Q-Plus T laser units because promotional materials on their website did not specify that certain claims did not apply to U.S. distributed devices.

    Product
    Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and 532 nm: Treatment of vascular lesions and pigmented lesions; Hair and tattoo removal; The incision, excision, ablation, vaporization of soft tissue for general dermatology. Ruby 694nm: Cutting, vaporization and abla
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-129-2013·2013-01-23

    James G. Cole Recalls I-C Drops Eye Cleansing Agent for Sterility Labeling

    James G. Cole, Inc. is recalling I-C Drops Eye Cleansing Agent because the label does not state the product is sterile, as required by FDA regulations.

    Product
    I-C Drops, Eye Cleansing Agent, 15 ml ASN/Maxam P.O. Box 1277 Hood River, OR 97031
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0692-2013·2013-01-23

    Quanta System Laser Recall for Inaccurate Promotional Website Claims

    Quanta System is recalling 12 Eterna Giovinezza laser units because its website contained promotional materials with claims not applicable to U.S. distributed devices.

    Product
    Eterna Giovinezza System, Powered Laser Surgical Instrument. Permanent hair reduction; Photocoagulation of dermatological vascular lesions; Photothermolysis of blood vessels (treatment of facial and leg veins); Treatment of benign pigmented lesions; Inflammatory acne
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0693-2013·2013-01-23

    Quanta System Laser Surgical Instrument Recall for Promotional Material Claims

    Quanta System is recalling 22 laser surgical instruments because website promotional materials contained claims not applicable to US devices.

    Product
    Ultrawave II EX 1320/ Ultrawave III EX 1320 Powered Laser Surgical Instrument. Nd:YAG 1064 nm: Coagulation and hemostasis of benign vascular lesions (e.g. port wine stains, hemangiomas, warts, telangiectasia, rosacea, venus lake, leg and spider veins, scars, straie and psoriasis
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0697-2013·2013-01-23

    IDS Recalls 25-Hydroxy Vitamin D EIA Due to QC Error

    IDS is recalling 25-Hydroxy Vitamin D EIA kits because a quality control report contained an incorrect calibrator value.

    Product
    25-Hydroxy Vitamin D EIA, Catalog #AC-57F1. Product Usage: The IDS 25-Hydroxy Vitamin D EIA kit is an enzymeimmunoassay intended for the quantitative determination of 25-hydroxyvitamin D (25-OH D) and other hydroxylated metabolites in human serum or plasma. Results are to be
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0675-2013·2013-01-23

    Philips CT System Software Recall for Coronary Artery Labeling Defect

    Philips is recalling 108 CT systems because a software defect prevents users from labeling coronary arteries in rendered images.

    Product
    Computed Tomography X-Ray System Brilliance Workspace Portal, Model #728269 Philips Medical Systems, Highland Heights, OH. The Brilliance Workspace Portal is a component of the Computed Tomography X-Ray System that is intended to produce cross-sectional images of the body by c
    Category
    Medical Device
    Distribution
    17 states
  • LowFDA (Drugs)·D-127-2013·2013-01-23

    Upsher Smith Recalls Divalproex Sodium Tablets Due to Labeling Error

    Upsher Smith is recalling 11,316 bottles of Divalproex Sodium Delayed-Release Tablets because some labels are missing the color-coded strength indicator.

    Product
    Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only, Manufactured by Upsher-Smith Laboratories, Inc., Minneapolis, MN 55447, NDC 0245-0182-11.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0865-2013·2013-01-16

    UNFI Recalls Kinnikinnick Gluten-Free Pie Crusts Due to Undeclared Eggs

    UNFI is recalling Kinnikinnick Gluten-Free Pie Crusts because they contain eggs that are not listed on the label.

    Product
    Kinnikinnick Pie Crust Gluten Free (frozen) weight 290 g/ 10 oz Qty/Pkg: 2, UPC 620133006229, Kinnikinnick Foods 10940 120 Street, Edmonton, AB Canada.
    Category
    Food
    Distribution
    4 states