The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 mis labeling recalls we have scored against our rubric, 161 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 589 (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.

6926–6950 of 9611

  • HighFDA (Food)·F-0478-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk and Shellfish Allergens

    Maine Natural Health, Inc. is recalling Recovery Chocolate dietary supplements because they fail to declare milk and shellfish allergens.

    Product
    Recovery Chocolate (also labeled Post Workout), Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0480-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Endurance Daily Vanilla Dietary Supplement because it fails to declare the milk allergen.

    Product
    Endurance Daily Vanilla Dietary Supplement Packaged under the label: Stronger Faster Healthier and Mainer Whey Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0498-2015·2014-11-19

    365 Organic Raisin Granola Recalled for Unlabeled Tree Nuts

    Whole Foods Market recalls 365 Organic Raisin Granola because it may contain pecans and coconut not listed on the label.

    Product
    365 Organic Raisin Granola in 17 ounce (482 gram) cardboard cartons; 12 cartons per case. UPC: 099482448738
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·F-0474-2015·2014-11-19

    Maine Natural Health Recalls Pure Whey Vanilla Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Pure Whey Vanilla dietary supplements because the packaging fails to declare the allergen milk.

    Product
    Pure Whey Vanilla , Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0481-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health is recalling Endurance Daily Chocolate dietary supplements because they fail to declare milk as an allergen.

    Product
    Endurance Daily Chocolate Dietary Supplement Packaged under the label: Stronger Faster Healthier Coconut, Lime Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0502-2015·2014-11-19

    Mondelez Recalls Chiclets Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0483-2015·2014-11-19

    Protein Supplement Recalled for Failing to Declare Milk Allergen

    Maine Natural Health, Inc. is recalling Endurance Pre Race Pina Colada dietary supplements because they fail to declare the milk allergen.

    Product
    Endurance Pre Race Pina Colada, Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0470-2015·2014-11-19

    Pride of Africa Semo Semolina Recalled for Undeclared Wheat

    Raymond-Hadley Corp. is recalling Pride of Africa brand Semo Semolina because label review revealed the product contains undeclared wheat.

    Product
    Pride of Africa brand Semo "Semolina", Net Wt. 5 lb., UPC 016712016918 --- A Product of Raymond-Hadley Corp. Spencer, NY 14883 1-800-252-5220
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0477-2015·2014-11-19

    Protein supplement recalled for undeclared milk and shellfish allergens

    Maine Natural Health, Inc. is recalling Recovery Vanilla dietary supplements because the labels fail to declare milk and shellfish allergens.

    Product
    Recovery Vanilla (also labeled Post Workout), Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0488-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Daily Balance Natural Dietary Supplement because it fails to declare milk as an allergen.

    Product
    Daily Balance Natural Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0500-2015·2014-11-19

    Mondelez Recalls Chiclets Peppermint Gum for Undeclared Soy Lecithin

    Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.

    Product
    1) Chiclets Peppermint Gum, 6-10 piece packages (60 pieces), Retail UPC 0 12546 10105 9; 2)Chiclets Peppermint Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02501 0, Case UPC 1001254 3)Chiclets Peppermint Gum, (12 pieces), Retail UPC 0 12546 10128 8; 4)Chiclets Pe
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0191-2015·2014-11-19

    Bard PerFix Light Plug Recalled for Labeling Mismatch

    Davol, Inc. is recalling 78 units of Bard PerFix Light Plug because the patient record label did not match the actual product in the packaging.

    Product
    Bard¿ PerFix Light Plug The Bard¿ PerFix Light Plug is indicated for reinforcement if soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0205-2015·2014-11-19

    Medtronic Launcher Coronary Guide Catheter Recalled for Incorrect Length

    Medtronic Vascular is recalling 11 Launcher Coronary Guide Catheters because they have a usable length of 90 cm instead of the labeled 55 cm.

    Product
    Medtronic Launcher Coronary Guide Catheter; MODEL: LA6JR40K
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0248-2015·2014-11-19

    Assured Naproxen Sodium Tablets Recalled Due to Mispackaging Error

    Contract Packaging Resources Inc. is recalling Assured Naproxen Sodium Tablets because correct labeled bottles of Assured Ibuprofen softgels were mistakenly packaged into Naproxen cartons.

    Product
    Assured Naproxen Sodium Tablets, USP 220 mg., 15 count bottle, Repackaged by Contract Packaging Resources, Inc 8009 Industrial Village Road Greensboro, NC 27409 Distributed by Greenbrier International, Inc Chesapeake, VA 23320
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0190-2015·2014-11-19

    Philips MX 16-slice CT Scanner Recalled for Incorrect Image Orientation

    Philips Medical Systems is recalling 708 MX 16-slice CT Scanner Systems because scan images may display left and right sides reversed, potentially leading to misinterpretation of patient position.

    Product
    MX 16-slice CT Scanner System and MX 16-slice CT Scanner System Phase 11 can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array with multi-slice capability up to 16 slices simultaneously. The acquired X-RAY tra
    Category
    Medical Device
    Distribution
    20 states
  • LowFDA (Devices)·Z-0207-2015·2014-11-19

    CooperSurgical MILEX Pessary Kits Recalled for Incorrect Expiration Date

    CooperSurgical is recalling 17 MILEX Pessary Kits because the packaging displays an incorrect expiration date.

    Product
    CooperSurgical MILEX PESSARY KITS-Ring w/Support Folding Pessary- #1 Model: MXKPRS01 Product Usage: The CooperSurgical Milex silicon pessary is a safe and effective device used to manage a number of gynecologic issues including pelvic support defects and stress urinary inc
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Devices)·Z-0208-2015·2014-11-19

    CooperSurgical MILEX Pessary Kits Recalled for Incorrect Expiration Date

    CooperSurgical is recalling 6 units of MILEX Pessary Kits due to incorrect expiration dates printed on the packaging.

    Product
    CooperSurgical MILEX PESSARY KITS- Hodge w/Support Folding Pessary- #1 Model: MXKPHS01 Product Usage: The CooperSurgical Milex silicon pessary is a safe and effective device used to manage a number of gynecologic issues including pelvic support defects and stress urinary
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Devices)·Z-0212-2015·2014-11-19

    Siemens IMMULITE Calcitonin Control Module Recalled for Typographical Error

    Siemens Healthcare Diagnostics is recalling the IMMULITE Calcitonin Control Module due to a typographical error in the expiration date on the instructions for use.

    Product
    IMMULITE Calcitonin Control Module (IMMULITE, IMMULITE 1000, IMMULITE 2000, IMMULITE 2000 XPi) For in vitro diagnostic use with IMMULITE¿ Systems Analyzers  for the quantitative measurement of calcitonin (thyrocalcitonin) in human serum or heparinized plasma, as an aid in the
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0177-2015·2014-11-12

    St. Jude Medical Recalls Electrophysiology Catheters Due to Incorrect Packaging

    St. Jude Medical is voluntarily recalling 26 electrophysiology catheters because the packaging contains the wrong device model. No serious injuries have been reported.

    Product
    St. Jude Medical, Fixed Curve Response 6F Electrophysiology Catheter, CSL, Model 401353
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-0464-2015·2014-11-12

    Mama Tere Sweet Corn Patties Recalled for Mislabeling

    Family Food Distributors, Inc. is recalling Mama Tere Arepa de Chocolo sweet corn patties because the products were found to be mislabeled.

    Product
    Mama Tere Arepa de Chocolo Sweet Corn Patty 10.5 oz/300g 4 units Product of Colombia Importado Por: Family Food Distributors, Inc. 969 Newark Turnpike, Unit D, Kearny, NJ 07032
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Food)·F-0466-2015·2014-11-12

    Mama Tere Arepa de Moto Hominy Patties Recalled for Mislabeling

    Family Food Distributors, Inc. is recalling Mama Tere Arepa de Moto Hominy Patties because the product was found to be mislabeled.

    Product
    Mama Tere Arepa de Moto Hominy Patty 14.1 oz / 400 g 5 units Product of Colombia Importado Por: Family Food Distributors, Inc. 969 Newark Turnpike, Kearny, NJ 07032 UPC 812828011652
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0162-2015·2014-11-12

    Merit Maestro Microcatheter Recalled for Incorrect Distal Tip Size

    Merit Medical Systems is recalling 56 Maestro Microcatheters because they were packaged with a 2.8 F distal tip instead of the labeled 2.4 F.

    Product
    Merit Maestro Microcatheter, 2.4F 130cm Straight, REF28MC24130ST, Rx Only, Non-pyrogenic Sterile if package is unopened or undamaged.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0164-2015·2014-11-12

    Siemens Calibrator E Recalled for Positive Bias in Cortisol and Progesterone Assays

    Siemens Healthcare Diagnostics is recalling Calibrator E kits due to positive bias in Cortisol and Progesterone assays on ADVIA Centaur Systems.

    Product
    Siemens Calibrator E; SMN 10309079 (2 pack), SMN 10321075 (6 pack), SMN 10335532 (6 pack Ref)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0234-2015·2014-11-12

    Obagi Nu-Derm Clear Prescription Cream Recalled for Labeling Error

    Obagi Medical Products is recalling 975 bottles of Obagi Nu-Derm Clear due to a labeling mix-up where Exfoderm Forte contents were shipped.

    Product
    OBAGI NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION — OBAGI NU-DERM SYSTEM NORMAL-OILY SKIN TRANSFORMATION (HYDROQUINONE, HOMOSALATE, OCTISALATE, ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0465-2015·2014-11-12

    Mama Tere Arepa Products Recalled for Mislabeling

    Family Food Distributors, Inc. is recalling Mama Tere Arepa products due to mislabeling. The affected items were distributed in six states.

    Product
    Mama Tere Arepa de Blanca de Maiz White Corn Patty 14.1 oz/400g 5 units Product of Colombia Importado Por: Family Food Distributors, Inc. 969 Newark Turnpike, Kearny, NJ 07032 UPC 812828011676
    Category
    Food
    Distribution
    6 states