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.

3951–3975 of 9607

  • ModerateFDA (Devices)·Z-0506-2018·2018-02-14

    Cardiovascular Systems Recalls Peripheral Diamondback Atherectomy Systems Due to Labeling Error

    Cardiovascular Systems Inc. is recalling eight units of the Peripheral Diamondback 1.50 Solid OAD system because labeling for two lots was potentially switched during production.

    Product
    Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0553-2018·2018-02-14

    Binding Site Rheumatoid Factor Kit Recalled for Control Value Deviations

    The Binding Site Group is recalling Rheumatoid Factor kits because low and high controls are returning results above assigned values.

    Product
    Rheumatoid Factor (RF) Kit for use on SPAPLUS, Product #LK151.S.A Intended for the quantitative in-vitro measurement of rheumatoid factor in serum using the Binding Site SPAPLUS analyser. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis. This t
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0505-2018·2018-02-14

    Cardiovascular Systems Recalls Peripheral Diamondback Atherectomy Systems Due to Labeling Error

    Cardiovascular Systems Inc. is recalling eight units of the Peripheral Diamondback 1.25 Solid OAD system because labeling for two lots was potentially switched during production.

    Product
    Peripheral Diamondback 1.25 Solid OAD, a percutaneous orbital atherectomy system indicated for use as therapy in patients with occlusive atherosclerotic disease in peripheral arteries and who are acceptable candidates for percutaneous transluminal atherectomy.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0548-2018·2018-02-14

    Astellas Recalls Mycamine Injection Vials Due to Labeling Error

    Astellas Pharma US Inc is recalling 63,600 vials of Mycamine (micafungin sodium) for Injection due to a label error on the declared strength.

    Product
    MYCAMINE — MYCAMINE (MICAFUNGIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0327-2018·2018-02-14

    Flawless Beauty Recalls Laroscorbine Platinum Vitamin C Due to Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Laroscorbine Platinum Vitamin C products because they were marketed without an approved NDA or ANDA.

    Product
    Laroscorbine Platinum Vitamin C 1 gm Collagen 0.35 gm, Roche
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0724-2018·2018-02-14

    Wienke's Market Hot Pepper Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Hot Pepper Jam because it contains butter, an ingredient not declared on the label.

    Product
    Wienke's Market Hot Pepper Jam, Net Wt. 8 oz (226g), UPC 14106-00221. Refrigerate after opening. Ingredients: sweet red peppers, onion, hot peppers, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0525-2018·2018-02-14

    ConvaTec Recalls Mislabelled Ostomy Skin Barrier Products

    ConvaTec is recalling a portion of Lot 7H02242 SUR-FIT Natura Moldable Durahesive Skin Barrier units that were incorrectly labeled as Natura Moldable Stomahesive Skin Barrier.

    Product
    SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible Collar, 10 pack, 45 mm, REF 411802. Intended for use as an ostomy protector providing a protective barrier to patient skin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0735-2018·2018-02-14

    Wienke's Market Strawberry Cherry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Strawberry Cherry Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Strawberry Cherry Jam, Net Wt. 8 oz (226g), UPC 14106-00234. Refrigerate after opening. Ingredients: strawberries, cherries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0747-2018·2018-02-14

    Wienke's Market Strawberry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market No Sugar Added Strawberry Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market No Sugar Added Strawberry Jam, Net Wt. 8 oz (226g), UPC 14106-00315. Refrigerate after opening. Ingredients: strawberries, rice syrup, grape juice, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0533-2018·2018-02-14

    MedComp Recalls CT Port Kits Packaged With Incorrect Needle Size

    Medical Components, Inc. is recalling 65 units of CT Port kits that were packaged with 21G needles instead of the labeled 18G needles.

    Product
    6.6F Plastic Dignity¿ Low Profile CT Port W/Attachable ChronoFlex¿ Polyurethane Catheter, Catalog # MRCTI66041, UDI#- 884908031157 Product Usage: Indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of medi
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-0772-2018·2018-02-14

    Titan Potato Puffs Recalled for Undeclared Sodium Bisulfite Ingredient

    Empresas Barsan, Inc. is recalling Titan Potato Puffs with Meat Flavor because the label fails to declare Sodium Bisulfite as an ingredient.

    Product
    TITAN, 6 rellenos, Potato Puffs with Meat Flavor, Net Weight 26.4 oz (748g)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0325-2018·2018-02-14

    Flawless Beauty Recalls Relumins Vitamin C Ampules for Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Relumins Vitamin C Solvent ampules because they were marketed without an approved NDA or ANDA.

    Product
    Relumins Vitamin C Solvent ampules
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0781-2018·2018-02-14

    Stevens Bakery Recalls No Sugar Added Pumpkin Pies for Missing Aspartame Warning

    Stevens Family Bakery & Orchard LLC is recalling No Sugar Added Pumpkin Pies because the labels failed to include the required warning statement for aspartame.

    Product
    No Sugar Added Pumpkin Pie Baked whole pies, Stevens Bakery & Orchard, 7344 Thackery Road, Springfield, Ohio 45502, (937) 788-2873
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0719-2018·2018-02-14

    Wienke's Market Cherry Rhubarb Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Cherry Rhubarb Jam because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Cherry Rhubarb Jam, Net Wt. 8 oz (226g), UPC 14106-00216. Refrigerate after opening. Ingredients: cherries, rhubarb, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0711-2018·2018-02-14

    Wienke's Blueberry Rhubarb Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Blueberry Rhubarb Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Blueberry Rhubarb Jam, Net Wt. 8 oz (226g), UPC 14106-00207. Refrigerate after opening. Ingredients: blueberries, rhubarb, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0721-2018·2018-02-14

    Wienke's Market Currant Jelly Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Currant Jelly because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market Currant Jelly, Net Wt. 8 oz (226g), UPC 14106-00219. Refrigerate after opening. Ingredients: currant juice, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0728-2018·2018-02-14

    Wienke's Market Hot Raspberry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Hot Raspberry Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Hot Raspberry Jam, Net Wt. 8 oz (226g), UPC 14106-00240. Refrigerate after opening. Ingredients: raspberries, sweet red peppers, onion, hot peppers, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0723-2018·2018-02-14

    Wienke's Market Gooseberry Jam Recalled for Undeclared Butter

    Wienke LLC is recalling Wienke's Market Gooseberry Jam because it contains butter that is not listed on the label.

    Product
    Wienke's Market Gooseberry Jam, Net Wt. 8 oz (226g), UPC 14106-00220. Refrigerate after opening. Ingredients: gooseberries, sugar, pectin.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0538-2018·2018-02-14

    Exactech Recalls Alteon HA Femoral Stems Due to Labeling Error

    Exactech is recalling 34 Alteon HA Femoral Stems because the labels incorrectly described the device. The units were distributed to five US states.

    Product
    Alteon HA Femoral Stem, Press-Fit, Extended Offset, Cementless, HA Coated, Collared, Size 5 All Exactech Hip Systems are indicated for use in skeletally mature individuals undergoing primary surgery for hip replacement due to osteoarthritis, rheumatoid arthritis, osteonecros
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-0739-2018·2018-02-14

    Wienke's Apple Butter Recalled for Undeclared Butter Ingredient

    Wienke LLC is recalling No Sugar Added Apple Butter because it contains butter, an ingredient not listed on the label.

    Product
    Wienke's Market No Sugar Added Apple Butter, Net Wt. 8 oz (226g), UPC 14106-00300. Refrigerate after opening. Ingredients: apples, cinnamon, cloves, allspice.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0814-2018·2018-02-14

    Olde Thompson BBQ Grinder Recalled for Incorrect Sodium Labeling

    Olde Thompson is recalling Sweet & Smoky BBQ Grinders because the label states 0 mg sodium, but the product contains 350 mg per serving.

    Product
    Olde Thompson Sweet & Smoky BBQ Grinder NET WT. 6.7 oz. (189.9g) Olde Thompson Oxnard, CA Ingredients: Sea Salt, demerara sugar, Dehydrated garlic, chili pepper, mustard seed, paprika, black pepper, oregano, coriander seed, cumin seed, natural hickory smoke flavor, thyme
    Category
    Food
    Distribution
    8 states
  • LowNHTSA·18V105000·2018-02-13

    Gulf Stream Recalls 2018 Matrix and Geo Trailers for Label Errors

    Gulf Stream is recalling 2018 Matrix and Geo recreational trailers because the Federal Certification Labels incorrectly list the rear axle weight rating.

    Product
    GULF STREAM — GULF STREAM MATRIX, GEO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0472-2018·2018-02-07

    Clopidogrel Tablets Recalled Due to Simvastatin Labeling Error

    International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.

    Product
    Clopidogrel Tablets, USP 75 mg, 30-count bottles, Rx only, Packaged for: International Laboratories, LLC St. Petersburg, FL 33710, NDC 54458-888-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0263-2018·2018-02-07

    Medline Catheter Care Tray Recalled for Subpotent Iodine Concentration

    Medline Industries is recalling lidded catheter care trays because the povidone-iodine prep pads contain less iodine than the label claims.

    Product
    Medline TRAY, CATHETER CARE, LIDDED. Packaged in USA for Medline Industries, Inc., Northfield, IL 60093
    Category
    Drug
    Distribution
    Distributed nationwide