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.

976–1000 of 9606

  • HighFDA (Food)·F-0047-2023·2022-10-26

    Trader Joe's Organic Tortilla Chip Rounds recalled for undeclared milk and soy

    Trader Joe's Organic Yellow Tortilla Chip Rounds may contain undeclared milk and soy allergens. The product contains small amounts of Spicy Cheese Crunchies which were not listed on the label.

    Product
    16 oz. bags of Trader Joe's Organic Yellow Tortilla Chip Rounds. UPC: 0074-0449 Distributed and Sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and sold exclusively by: Trader Joe's, Monrovia, CA 91016 Distributed and Sold Exclusively By: Trader Joe's, Monro
    Category
    Food
    Distribution
    16 states
  • HighFDA (Food)·F-0066-2023·2022-10-26

    Mrs. Freshley's Cherry Fruit Pie recalled for undeclared soy lecithin

    Flowers Foods is recalling Mrs. Freshley's Cherry Fruit Pie due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume the product.

    Product
    Mrs. Freshley's Cherry Fruit Pie NET WT 4.5 OZ (128g) UPC 0 72250 0081 0 DISTRIBUTED BY FLOWERS FOODS SPECIALTY GROUP, LLC, 5987 SOUTH ROYAL ATLANTA DR, TUCKER, GA 30084
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0102-2023·2022-10-26

    ARROW Midline Catheter Kit Mislabeled with Wrong Device Type

    ARROW INTERNATIONAL Inc. is recalling an ARROW Pressure Injectable Arrowgard Blue Advance Midline Catheter Kit due to mislabeling. The package labels incorrectly specify a double-lumen 5.5 French catheter, but the kit contains a single-lumen 4.5 French catheter.

    Product
    ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0048-2023·2022-10-26

    Seeking Health Optimal Multivitamin Chewable Supplement Recalled for Excess Copper

    Seeking Health LLC is recalling Optimal Multivitamin Chewable Dietary Supplement tablets because lab testing found higher copper levels than stated on the label.

    Product
    Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product is packaged in white non-flex plastic bottles. UPC: 810007520902. Product labels read in part: Adults and children age 4 and over; Chew 2 tablets daily. Servi
    Category
    Consumer Product
    Distribution
    51 states
  • HighFDA (Food)·F-0049-2023·2022-10-26

    Karlsburger Kitchens beef gravy mix recalled for undeclared gluten

    Karlsburger Kitchens beef gravy mix is recalled for containing undeclared gluten despite its gluten-free label. The product poses a risk to consumers with celiac disease or gluten sensitivity.

    Product
    Karlsburger Kitchens NSLP 140 Beef Gravy Mix, Gluten Free. Packaged in the following sizes: 1. Item 32312. Net Weight 12 oz (340 gm) 2. Item 32325. Net Weight 25 lb. (11.34 kg). Manufactured in a plant that handles Gluten. Karlsburger Foods, Inc Monticello, MN 55362.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0068-2023·2022-10-26

    Tastykake Glazed Caramel Apple Pie Recalled for Undeclared Soy

    Flowers Foods is recalling Tastykake Glazed Caramel Apple Pie because some packages contain undeclared soy lecithin, a major food allergen. Consumers with soy allergies should not consume this product.

    Product
    TASTYKAKE GLAZED CARAMEL APPLE PIE NET WT 4.5 OZ (128g) UPC 0 25600 08618 6 DISTRIBUTED BY TASTY BAKING COMPANY, PHILADELPHIA, PA 19112
    Category
    Food
    Distribution
    50 states
  • HighFDA (Devices)·Z-0096-2023·2022-10-26

    Laryngeal mask airway recalled for incorrect size marking

    Intersurgical Solus Standard size 3 laryngeal mask airways are marked with incorrect size 4 information, which may cause misuse or improper sizing of the airway device.

    Product
    Intersurgical Solus Standard, laryngeal mask airway, size 3, small adult, 30-50kg Model Number: 8003000
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0014-2023·2022-10-26

    OTC Sinus Pressure and Pain Cough Product Mislabeled as Decongestant-Free

    Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.

    Product
    SINUS PRESSURE, PAIN AND COUGH — SINUS PRESSURE, PAIN AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0030-2023·2022-10-19

    Hobbs Helical Retrieval Basket Recall Due to Incorrect Expiration Date

    Hobbs Medical is recalling Helical Retrieval Baskets (Catalog 4822) with incorrect expiration dates on device labels. The mislabeled dates extend the shelf life, risking use of expired devices that may not perform as intended.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4822
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2023·2022-10-19

    Hobbs Posi-Stop Injection Needle recalled for incorrect expiration date labeling

    Hobbs Medical recalled Posi-Stop Injection Needles with incorrect expiration dates on labels, potentially allowing use of units past actual expiration. The recall affects 17 units distributed in the US and several countries.

    Product
    Hobbs Posi-Stop Injection Needle Catalog Number: 4722
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0054-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit: Incorrect Expiration Date on Device Labels

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits with incorrect expiration dates on labels that may extend shelf life beyond the actual expiration date.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0041-2023·2022-10-19

    Hobbs Medical Recalls Biliary Stent Kits Due to Mislabeled Expiration Dates

    Hobbs Medical, Inc. is recalling Biliary Pigtail Stent Kits with incorrect expiration dates displayed on device labels. Affected devices distributed from March 2018 through September 2020 may be used beyond their validated shelf life.

    Product
    Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0061-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Dates

    Hobbs Medical recalled Freeman Pancreatic Flexi-Stent devices due to incorrect expiration dates on labels that extend the shelf life, potentially allowing use beyond intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0036-2023·2022-10-19

    Hobbs Retrieval Forceps Recalled for Incorrect Expiration Dates

    Hobbs Medical is recalling Retrieval Forceps with incorrect expiration dates on device labels. Affected devices distributed between March 2018 and September 2020 may be used past their actual expiration.

    Product
    Hobbs Retrieval Forceps Catalog Number: 5018
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0064-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent recalled for incorrect expiration date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels that extend perceived shelf life beyond actual device longevity.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6582
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0066-2023·2022-10-19

    Freeman Pancreatic Stent Recall: Incorrect Expiration Date on Device Labels

    Freeman Pancreatic Flexi-Stents with incorrect expiration dates on labels may be used beyond their validated shelf life. The recall affects devices distributed in the US and five other countries from March 2018 through September 2020.

    Product
    Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0010-2023·2022-10-19

    Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date

    Hobbs Medical is recalling Spray Catheter devices due to incorrectly labeled expiration dates that extend shelf life beyond the actual safe-use period. The recall affects 275 units distributed between March 2018 and September 2020.

    Product
    Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For endoscopy procedures Ref: 2190
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0053-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kits Recalled for Incorrect Expiration Dates

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kits due to labeling errors showing incorrect expiration dates that extend the shelf life of affected devices.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6567) Catalog Number: 6519
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0019-2023·2022-10-19

    Hobbs Scope Introducer Recalled for Incorrect Label Expiration Date

    Hobbs Medical is recalling 140 units of its Hobbs Scope Introducer due to incorrect label expiration dates that extend the shelf life. Affected devices were distributed in the US and internationally from March 2018 to September 2020.

    Product
    Hobbs Scope Introducer Catalog Number: 4650
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0046-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit recalled for incorrect expiration date labeling

    Hobbs Medical recalls the Freeman Pancreatic Flexi-Stent Kit due to incorrect expiration dates on product labels that extend shelf life. Affected devices were distributed to the US and international markets from March 2018 through September 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0051-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit Recalled for Mislabeled Expiration Date

    Hobbs Medical recalls Freeman Pancreatic Flexi-Stent Kit units with incorrect expiration dates on labels, extending apparent shelf life. Units distributed in the US and Canada, Austria, Belgium, Finland, and Norway from 2018–2020 are affected.

    Product
    Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0045-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits Recalled Due to Incorrect Expiration Date Label

    Hobbs Medical is recalling Biliary Pigtail Stent Kits distributed from March 2018 to September 2020 due to incorrect expiration date labels that extend the shelf life beyond the actual safe period.

    Product
    Hobbs Biliary Pigtail Stent Kits Catalog Number: 6108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0013-2023·2022-10-19

    Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Dates

    Hobbs Medical is recalling its Cytology Brush (catalog 4204) because device labels show incorrect expiration dates that extend the claimed shelf life. Affected devices were distributed in the US and several other countries from March 2018 to September 2020.

    Product
    Hobbs Medical Cytology Brush Catalog Number: 4204
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent label displays incorrect expiration date

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on their labels. The labeling error extends the shelf life beyond the intended timeframe.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6584
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0082-2023·2022-10-19

    Prismaflex M Set Medical Device Recalled Due to Instruction Mistranslation

    Baxter Healthcare is recalling 334,932 Prismaflex M Set M150 devices due to a mistranslation in instructions that creates contradictory information about patient body weight restrictions.

    Product
    Prismaflex M Set: M150 (product code 109990). For use in providing continuous fluid management and renal replacement therapies.
    Category
    Medical Device
    Distribution
    Distributed nationwide