The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 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.

1476–1500 of 9607

  • ModerateFDA (Devices)·Z-1532-2021·2021-05-12

    Medtronic Abre Venous Self-expanding Sent System Recall for Incorrect Size Labeling

    Medtronic is recalling 23 Abre Venous Self-expanding Sent Systems because the device size is incorrectly printed on the device itself, though the packaging is labeled correctly.

    Product
    Medtronic Abre Venous Self-expanding Sent System, Catalog number REF AB9U16080090 - Product Usage: intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0479-2021·2021-05-12

    Natrol Melatonin 3 mg Tablets Recalled for Mislabeling as ALA 300 mg

    Natrol LLC is recalling one lot of Melatonin 3 mg tablets that were mislabeled as ALA 300 mg capsules. The recall covers 12,740 units distributed across multiple US states and international locations.

    Product
    Natrol Melatonin 3 mg, Tab 60 White bottle with purple flip-top cap. Fall asleep faster, Stay asleep longer, 100$ Drug Free 1 Tablet 20 minutes before bedtime. Manufactured by Natrol LLC. Chatsworth, CA 91311 USA
    Category
    Drug
    Distribution
    36 states
  • HighFDA (Food)·F-0467-2021·2021-05-05

    Champlain Chocolate Company Recalls Organic Mr. Goodtime Bunny for Undeclared Almonds

    Champlain Chocolate Company is recalling Organic Mr. Goodtime Bunny chocolate products because they may contain undeclared almonds. The recall affects 443 units distributed in nine states.

    Product
    Organic Mr. Goodtime Bunny***NET WT 3.35 LBS (1.4kg)***INGREDIENTS: *Milk, *Dark, AND *WHITE CHOCOLATE (*SUGAR, *MILK POWDER, *COCOA BUTTER, *CHOCOLATE LIQUOR, *COCOA POWDER (PROCESSED WITH ALKALI), *SOYBEAN LECITHIN, *VANILLA EXTRACT, AND *VANILLA POWDER). CONTAINS MILK AND SOYB
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-0469-2021·2021-05-05

    Richelieu Foods Recalls Tuscan Garden Ranch Dressing Due to Labeling Error

    Richelieu Foods is recalling Tuscan Garden Ranch Dressing sold at ALDI because incorrect labels failed to disclose milk and egg ingredients.

    Product
    Tuscan Garden Ranch Dressing, packaged in 16 oz bottles, Dist. & Sold Exclusively by ALDI, Batavia, IL packaged in 12 bottles per case
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0458-2021·2021-05-05

    Torn & Glasser Recalls Dark Chocolate Espresso Beans for Undeclared Walnuts

    Torn & Glasser, Inc. is recalling Dark Chocolate Espresso Beans because the product contains walnuts that are not declared on the label.

    Product
    Dark Chocolate Expresso Beans; Net Wt. 12 oz. (340g), Best if used by 11-19-2021. Contains Soy, May Contain Milk. Packed in a facility that processes on share equipment with Peanuts, Tree Nuts, Milk, Wheat and Egg. UPC: 0 72488 99868 1 Packed by Torn & Glasser, Los An
    Category
    Food
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-1493-2021·2021-05-05

    Cytocell Recalls Chromosome X Alpha-Satellite Probes Due to Cross-Reactivity

    Cytocell Ltd. is recalling 89 Chromosome X Alpha-Satellite probes because users may observe additional signals at 9q34, contradicting the insert.

    Product
    Chromosome X Alpha-Satellite in FITC Spectrum - Product Usage: Analyte Specific Reagents. Model: MPA3481
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1516-2021·2021-05-05

    Smiths Medical Recalls ACE MDI Spacers Due to Labeling Errors

    Smiths Medical ASD Inc. is recalling 250 units of ACE MDI Spacers with Small Masks because shipping box labels may be incorrect.

    Product
    ACE MDI Spacer with Small Mask - Product Usage: designed to assist with the delivery of aerosolized medications from metered dose inhaler canisters and with mechanically ventilated patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1489-2021·2021-05-05

    Ortho-Clinical VITROS Black Reference Slides Recalled for Mislabeling

    Ortho-Clinical Diagnostics is recalling VITROS Black Reference Slides incorrectly labeled as White Reference Slides, which may cause analyzer delays.

    Product
    VITROS¿ Black Reference Slides CATALOG #: J02316 - Product Usage: The Black Reference Slide is a part/ tool used in the reflectometer correction factor adjustment procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1515-2021·2021-05-05

    Smiths Medical Recalls Palm Cups Due to Incorrect Shipping Box Labels

    Smiths Medical ASD Inc. is recalling 682 Palm Cups because shipping box labels may be incorrect. The devices are intended to mobilize bronchial secretions.

    Product
    Palm Cups - Product Usage: intended to be used to percuss the chest wall to mobilize the secretions within the bronchial tree.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2021·2021-05-05

    Cardiac Assist Recalls Incorrectly Packaged Protek Solo Venous Dilator Sets

    Cardiac Assist, Inc. is recalling 13 Protek Solo Venous Dilator Sets due to incorrect packaging discovered in finished goods.

    Product
    Protek Solo Venous Dilator Set: dilator, vessel, for percutaneous catheterization. Catalog #: 5840-2417 - LS Tandem Life Kit - V24/A17 Catalog #: 5840-2415 - LS Tandem Life Kit - V24/A15 Catalog #: 5740-2417 - TandemLife Kit - V24/A17 Catalog #: 5100-1422 - ProtekSolo Venous
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1494-2021·2021-05-05

    Coltene Whaledent Recalls TMS LINK PLUS Self-Threading Dental Pins

    Coltene Whaledent Inc is recalling TMS LINK PLUS Self-Threading Dental Pins because incorrect pins were packaged and distributed. The recall affects 65 packs of 20 pins.

    Product
    Dental pins - TMS LINK PLUS Self-Threading Pins - Product Usage: implanted into the teeth or for lab use for dental restoration purposes. The normal procedure requires a hole to be drilled into the tissue of a tooth with an intraoral drill prior to installation. Model number/Cata
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1510-2021·2021-05-05

    Smith & Nephew Recalls Mislabeled CANNU-Flex SILK Interference Screws

    Smith & Nephew is recalling CANNU-Flex SILK Interference Screws because some boxes were mislabeled, containing 6mm x 20mm screws instead of the labeled 6mm x 30mm size.

    Product
    CANNU-Flex SILK Interference Screws 6 mmx 30 mm - Product Usage: used for interference fixation of bone-tendon-bone of soft tissue grafts in anterior cruciate ligament reconstruction, Part Number: 014208
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1502-2021·2021-05-05

    Medela AXS Universal Aspiration Tubing Recalled for Incorrect Expiration Date

    Medela is recalling AXS Universal Aspiration Tubing because the label displays an incorrect expiration date of 2023-07-24 instead of 2021-07-24.

    Product
    Stryker Medela REF 077.0193 AXS Universal Aspiration Tubing (01)07612367053921 - Product Usage: AXS Universal Aspiration Tubing is used with the Dominant Flex Surgical Suction Pump.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2021·2021-05-04

    Bellisio Recalls Spaghetti with Meat Sauce for Undeclared Soy Allergen

    Bellisio Foods is recalling approximately 3,927 pounds of Michelina's Spaghetti with Meat Sauce due to misbranding and an undeclared soy allergen.

    Product
    Bellisio Foods, Inc. — Bellisio Foods, Inc. Recalls Beef Pasta Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·016-2021·2021-05-01

    Hempstead Foodservice Recalls Pork Chops for Undeclared Soy Allergen

    Hempstead Foodservice is recalling pork chops because they contain undeclared hydrolyzed soy protein, a known allergen.

    Product
    Hempstead Foodservice Inc. — Hempstead Foodservice Recalls Pork Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighCPSC·21740·2021-04-29

    Modernist Pantry Recalls Sodium Hydroxide for Packaging and Labeling Defects

    Modernist Pantry is recalling Kitchen Alchemy Sodium Hydroxide products because the packaging is not child-resistant and labels violate federal hazardous substance requirements.

    Product
    Modernist Pantry Kitchen Alchemy Sodium Hydroxide
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0453-2021·2021-04-28

    Rise Baking Recalls Dawn Cookies and Creme Cakes for Undeclared Hazelnut

    Rise Baking Company is recalling Dawn 3 Layer Cookies and Creme Cakes because the label fails to list hazelnut as an ingredient.

    Product
    Dawn Food Products,8 3 Layer Cookies and Creme Cake , 35 oz., cake is placed on a cardboard plate which is then placed on a plastic plate and closed in a plastic dome, 6 cakes per case , Keep frozen for storage. Store refrigerated or ambient for sale and use.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0452-2021·2021-04-28

    Rise Baking Company Recalls Vanilla Bean Waterfall Cakes for Undeclared Hazelnut

    Rise Baking Company is recalling Dawn Food Products 7 1/2 Layer Vanilla Bean Waterfall Cakes because the label fails to list hazelnut as an ingredient.

    Product
    Dawn Food Products, 7 2 Layer Vanilla Bean Waterfall Cake, 35 oz., cake is placed on a cardboard plate which is then placed on a plastic plate and closed in a plastic dome, 6 cakes per case , Keep frozen for storage. Store refrigerated or ambient for sale and use.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0454-2021·2021-04-28

    Reser's Macaroni Salad Recalled for Undeclared Wheat and Egg Allergens

    Reser's Fine Foods is recalling Freshness Guaranteed Macaroni Salad Amish because the bottom label incorrectly identifies the product as Red Potatoes or Baked Beans, failing to declare wheat and egg allergens.

    Product
    Freshness Guaranteed Macaroni Salad Amish, item # 579284, refrigerated, packaged in a clear cup with clear snap on lid, net wt. 32 oz. UPC 0 78742 13235 8. Each master case containing 6/32 oz. packages. Distributed by: Walmart Inc, Bentonville, AR. The CORRECT label is read i
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1440-2021·2021-04-28

    Medtronic Endoskeleton TC Interbody System Recalled for Packaging Labeling Error

    Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes were mislabeled, containing the wrong size device.

    Product
    Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Large, 8 mm, Product Number 5146-1608-N - Product Usage: indicated to be used with supplemental fixation cleared by the FDA for use in the cervical spine and autograft bone, allograft bone comprise
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0434-2021·2021-04-28

    Tropicana Recalls KeVita Cucumber Rosemary Kombucha Due to Mislabeling

    Tropicana Products, Inc. is recalling 5,479 cases of KeVita Cucumber Rosemary kombucha due to mislabeling of the bottled product inside the case.

    Product
    KeVita Cucumber Rosemary (primary package), 15.2 oz., glass bottles, 6 packages per case, refrigerated storage
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Food)·F-0449-2021·2021-04-28

    Motha Jelly Crystals Recalled for Undeclared Red Dye

    USA Lanka Inc. is recalling Motha Jelly Crystals Strawberry Flavoured Jelly because it contains undeclared FD&C Red #40.

    Product
    Motha Jelly Crystals Strawberry Flavoured Jelly , Net Wt. 100g
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-1439-2021·2021-04-28

    Medtronic Endoskeleton TC Interbody System Recalled for Incorrect Size Labeling

    Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes misidentify the size of the contained device.

    Product
    Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Small, 8 mm, Product Number 5146-1208-N - Product Usage: indicated to be used with supplemental fixation cleared by the FDA for use in the cervical spine and autograft bone, allograft bone comprise
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0446-2021·2021-04-28

    Motha Jelly Crystals Recalled for Undeclared Dyes and Unapproved Colorant

    USA LANKA INC is recalling Motha Jelly Crystals because the product contains undeclared FD&C yellow #5 and blue #1, as well as the unapproved dye carmoisine.

    Product
    Motha Jelly Crystals - Mixed Fruit Flavoured Jelly, Net Wt. 100g,
    Category
    Food
    Distribution
    10 states