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.

8851–8875 of 9622

  • LowFDA (Food)·F-1266-2013·2013-04-03

    Kettle Brand Honey Roast Nuts and Fruit Trail Mix Recalled for Sulfur Dioxide

    Kettle Foods is recalling Honey Roast Nuts and Fruit Trail Mix because it was made with dried pineapple containing sulfur dioxide instead of untreated pineapple.

    Product
    Item #1900 Kettle Brand Honey Roast Nuts and Fruit Trail Mix UPC 8411401900 Label reads in part "8411401900 Honey Roast Nuts & Fruit Mix Net Weight 24 Lbs. ***"
    Category
    Food
    Distribution
    0 states
  • LowFDA (Devices)·Z-1008-2013·2013-04-03

    Cooper Surgical Incontinence Pessary Recalled for Mislabeled Outer Packaging

    Cooper Surgical is recalling 31 units of Incontinence Dish Folding Pessaries because the outer packaging may not reflect the actual product size.

    Product
    Cooper Surgical Incontinence Dish Folding Pessary #0, 55mm. Milex Part Number: MXPCOND00 A pessary is a medical device that is inserted into the vagina to function as a supportive structure of the uterus and/or bladder and rectum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1006-2013·2013-04-03

    Cooper Surgical Incontinence Dish Pessary Recalled for Mislabeled Outer Packaging

    Cooper Surgical is recalling 45 units of Incontinence Dish pessaries because the outer package may not reflect the actual product size.

    Product
    Cooper Surgical Incontinence Dish w/ Support Pessary #0, 55mm. Milex Part Number: MXKPCONDS00 A pessary is a medical device that is inserted into the vagina to function as a supportive structure of the uterus and/or bladder and rectum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1012-2013·2013-04-03

    Cooper Surgical Cube Pessary Recalled Due to Mislabeled Outer Packaging

    Cooper Surgical is recalling 20 units of Cube Pessaries because the outer packaging may not reflect the actual product size.

    Product
    Cooper Surgical Cube Pessary w/Drainage Holes #0"1", 25mm. Milex Part Number: MXKPECH00 A pessary is a medical device that is inserted into the vagina to function as a supportive structure of the uterus and/or bladder and rectum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1007-2013·2013-04-03

    Cooper Surgical Incontinence Dish Folding Pessary Mislabeled Size Recall

    Cooper Surgical is recalling Incontinence Dish Folding Pessaries because the outer package may not reflect the actual product size.

    Product
    Cooper Surgical Incontinence Dish Folding Pessary #0, 55mm. Milex Part Number: MXKPCOND00 A pessary is a medical device that is inserted into the vagina to function as a supportive structure of the uterus and/or bladder and rectum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1229-2013·2013-03-27

    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Recalled for Allergen Mislabeling

    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System is being recalled because the label declares whey but fails to declare milk.

    Product
    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Lemonade 3.5 lb Manufactured & Distributed by Dymatize Enterprises, LLC, 13737 N. Stemmons FWY. Dallas, TX 75234 UPC 705016895649
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1231-2013·2013-03-27

    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Recalled for Undeclared Milk

    Dymatize Enterprises is recalling specific lots of XPAND Post Xtreme Mass Recovery System because the label declares whey but fails to declare milk.

    Product
    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Blue Raspberry 3.5 lb Manufactured & Distributed by Dymatize Enterprises, LLC, 13737 N. Stemmons FWY. Dallas, TX 75234 UPC 705016895601.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1230-2013·2013-03-27

    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Recalled for Undeclared Milk

    Dymatize Enterprises is recalling specific lots of XPAND Post Xtreme Mass Recovery System Fruit Punch because the label declares whey but fails to declare milk.

    Product
    Dymatize Nutrition XPAND Post Xtreme Mass Recovery System Fruit Punch 3.5 lb Manufactured & Distributed by Dymatize Enterprises, LLC, 13737 N. Stemmons FWY. Dallas, TX 75234 UPC 705016895625.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1208-2013·2013-03-27

    Ron's Pizza Warehouse Recalls Unlabeled Pizza Dough Shells Containing Wheat

    Ron's Pizza Warehouse is recalling approximately 700 pizza dough shells in Ohio because the product contains wheat but lacks allergen labeling.

    Product
    The pizza dough shells come in 5 lb. brown cardboard boxes, containing 25 shells per box.
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0967-2013·2013-03-27

    Alphatec ILLICO Spinal Rods Recalled for Incorrect Length Marking

    Alphatec Spine is recalling 7 ILLICO spinal rods that were laser-etched as 110mm but are actually 100mm long.

    Product
    ILLICO Straight CP TI Rod, -5.5MM x 110M; REF#73601-110; Qty 1; LBL-005; REV.B; RX ONLY; Alphatec Spine, Inc. The ILLICO¿ MIS Posterior Spinal Fixation System is intended to facilitate the surgical correction of non-cervical spinal deformities by providing temporary internal fix
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0973-2013·2013-03-27

    Keystone Dental Recalls Mislabeled PrimaConnex Tapered Dental Implants

    Keystone Dental Inc is recalling 120 units of PrimaConnex Tapered Implants because the included cover screw was a WD type instead of the labeled SD type.

    Product
    PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed bridgework.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0958-2013·2013-03-27

    Beckman Coulter Recalls Creatinine Reagents for Calibration Instructions

    Beckman Coulter is recalling Creatinine reagents to provide updated instructions for calibration stability and quality control frequency.

    Product
    Creatinine, Part Numbers OSR6178, OSR6678 Product Usage: System reagent for the quantitative determination of Creatinine in human serum and urine on Beckman Coulter AU analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0964-2013·2013-03-27

    Stryker Specialty Triathlon Knee Sizer Adjustment Housing Recalled for Fit and Marking Errors

    Stryker is recalling four units of Specialty Triathlon Knee Sizer Adjustment Housings because the standard femoral stylus does not fit and the left/right markings on the right sizer are reversed.

    Product
    Howmedica Osteonics Corp. Stryker Orthopaedics Specialty Triathlon Left and Right A//P Sizer Adjustment Housing PER File K2401. For use in knee prosthesis implantation. NON-STERILE
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0956-2013·2013-03-27

    Synthes Recalls Four Mis-etched Variable Angle Locking Compression Plates

    Synthes USA is recalling four Variable Angle Locking Compression Plates that were incorrectly etched with the wrong part number.

    Product
    Variable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate, Part Number 02.115.431. Indicated for: Dorsally displaced fractures, Open joint reconstruction, and Corrective osteotomies after distal radius malunion.
    Category
    Medical Device
    Distribution
    4 states
  • LowFDA (Devices)·Z-0970-2013·2013-03-27

    Agfa X-Ray Image Plate Recall Due to Incorrect Barcode Labeling

    Agfa Corp. is recalling 17 X-ray image plates shipped with incorrect size barcodes, affecting facilities in 10 US states.

    Product
    CR MD1.0 General Set, x-ray imager image plate. CR 10-X Image Plate 35CM X 43CM. An image plate, contained in an X-Ray cassette, used to capture images from X-Ray exposures. The cassette with the image plate, once exposed, is inserted in the Agfa Digitizer CR 10-X where the ima
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-208-2013·2013-03-27

    Novartis Recalls Nupercainal Ointment Due to Illegible Labeling

    Novartis Consumer Health is recalling Nupercainal Ointment because lot numbers and expiration dates may be illegible or missing.

    Product
    Nupercainal, Dibucaine, Hemorrhoidal & Topical Analgesic Ointment, a) 1-oz. tubes (NDC 0067-5812-96), b) 2-oz. tubes (NDC 0067-5812-86), OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-201-2013·2013-03-27

    West-ward Recalls Carisoprodol Tablets for Missing C-IV Labeling

    West-ward Pharmaceutical Corp. is recalling 1,763 bottles of Carisoprodol Tablets, 350 mg, because they lack the required C-IV imprint on the label.

    Product
    Carisoprodol Tablets, USP, 350 mg Rx Only, 100 tablets per bottle, Rx Only, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ 07724, NDC 0143-1176-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0966-2013·2013-03-27

    Volk Optical Recalls 20 Diopter Binocular Indirect Ophthalmoscope Lenses

    Volk Optical Inc is recalling 40 units of 20 Diopter Binocular Indirect Ophthalmoscope lenses due to mixed-up lot number engravings on the devices and packaging.

    Product
    20 Diopter Binocular Indirect Ophthalmoscope (BIO) Lens For visualization during diagnosis and laser therapy of the human retina (fundus) using a binocular indirect ophthalmoscope.
    Category
    Medical Device
    Distribution
    6 states
  • LowFDA (Drugs)·D-211-2013·2013-03-27

    Novartis Recalls 4 Way Saline Moisturizing Mist Due to Labeling Errors

    Novartis Consumer Health is recalling 4 Way Saline Moisturizing Mist bottles because lot numbers or expiration dates may be illegible or missing.

    Product
    4 way Saline Moisturizing Mist with Eucalyptol & Menthol, 1-fl. oz. bottles, OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-207-2013·2013-03-27

    Novartis Recalls Myoflex Cream Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling Myoflex Pain Relieving Cream because lot numbers and expiration dates may be illegible. The recall covers 2-oz and 4-oz tubes distributed nationwide and in Panama.

    Product
    Myoflex (trolamine salicylate) 10%, Pain Relieving Cream, a) 2-oz tube, b) 4-oz. tube, OTC. The firm name on the label is Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-210-2013·2013-03-27

    Novartis Recalls Nasal Spray Due to Illegible Lot and Expiration Dates

    Novartis Consumer Health is recalling 4 way Nasal Decongestant Menthol Nasal Spray because lot numbers and expiration dates may be illegible.

    Product
    4 way Nasal Decongestant Menthol Nasal Spray, containing phenylephrine hydrochloride 1%, a) 1/2-fl. oz. bottles (NDC 0067-2087-05) b) 1-fl. oz. bottles (NDC 0067-2087-01), OTC. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ 07054.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-209-2013·2013-03-27

    Novartis Recalls 4 Way Nasal Spray Due to Illegible Labeling

    Novartis Consumer Health is recalling 4 Way Nasal Spray because lot numbers and expiration dates may be illegible.

    Product
    4 WAY — 4 WAY (PHENYLEPHRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0974-2013·2013-03-27

    Intio ClearStart-SVM User Manual Recalled for Editing Mistake

    Intio Inc. is recalling seven copies of the ClearStart-SVM User Manual due to an editing mistake that could be interpreted as promoting an unapproved use.

    Product
    INTIO Inc., ClearStart-SVM Segmentation and Volumetric Measurement System, Users Manual. Part #: UM-06-20-0003. ClearStart-SVM is used for patient assessment using CT (computed tomography) images, in order to plan potential therapies or monitor tumor response to treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1061-2013·2013-03-20

    See's Candies Recalls Divinity Easter Eggs for Potential Peanut Mislabeling

    See's Candies is recalling 1.7 oz Divinity Easter Eggs with Walnuts because they may contain peanut butter instead of walnuts.

    Product
    See's Candies, Divinity with Walnuts; Net Wt. 1.7 oz, (48 gr). See's Candies, South San Francisco, CA.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1191-2013·2013-03-20

    Bay Valley Foods Recalls Pasta Mix for Missing Soy Labeling

    Bay Valley Foods is voluntarily recalling approximately 430,227 cases of boxed pasta mix products because the labeling did not include soy lecithin in the ingredient statement.

    Product
    55613130643 Our Specialty Linguini & Parmesan, Linguini pasta with naturally flavored Parmesan & Romano Cheese Sauce Mix, Net WT 5.8 oz ( 164g), UPC 0 55049 00602 5, Distributed by S.T. Specialty Foods, Inc, Brooklyn Park, MN 55455.
    Category
    Food
    Distribution
    21 states