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.

7176–7200 of 9611

  • SevereFDA (Devices)·Z-2021-2014·2014-07-30

    Blood Glucose Test Strips Recalled for Inappropriate Labeling and Marketing

    Diabetic Supply of Suncoast, Inc. is recalling Advocate Redi-Code+ blood glucose test strips because they were inappropriately labeled and marketed.

    Product
    ADVOCATE Redi-Code+ BMB-BA006A Blood Glucose test strips Product Usage: The ADVOCATE¿ Redi-Code+ BMB-BA006A Blood Glucose test strips are used only with the ADVOCATE¿ Redi-Code+ BMB-EA004S meter to quantitatively measure glucose in fresh capillary whole blood samples drawn fr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1448-2014·2014-07-30

    Shamrock Recalls Metformin ER Tablets Labeled as Immediate Release

    Shamrock Medical Solutions is recalling metformin ER tablets that were incorrectly labeled as immediate release. The mislabeling could lead to incorrect dosing.

    Product
    metFORMIN ER Tablets, 500 mg, Rx, Packaged and labeled as metFORMIN Immediate Release (IR), Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfr: Amneal/Interpharm, Hauppauge, NY NDC 53746-178-01
    Category
    Drug
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1449-2014·2014-07-30

    Shamrock Medical Recalls Mislabelled Pramipexole Tablets Packaged as Nebivolol

    Shamrock Medical Solutions is recalling Pramipexole Dihydrochloride tablets that were incorrectly labeled as Nebivolol. The error poses a risk of patients receiving the wrong medication.

    Product
    Pramipexole Dihydrochloride Tablets, 0.5 mg, Rx, packaged and labeled to contain Nebivolol tablets, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Northstar Rx, Memphis, TN NDC 16714-586-01
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-1450-2014·2014-07-30

    Shamrock Recalls Mislabelled Sulfamethoxazole and Trimethoprim Tablets

    Shamrock Medical Solutions Group LLC is recalling Sulfamethoxazole and Trimethoprim tablets due to a labeling error where 800 mg/160 mg tablets were labeled as 400 mg/80 mg.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2087-2014·2014-07-30

    Synthes Orthopedic Guide Blocks Recalled for Incorrect Labeling

    Synthes, Inc. is recalling 180 Guide Blocks for the Volar Distal Radius Plate System due to incorrect package labeling. The physical parts are correctly marked, but the packaging may identify the wrong side.

    Product
    Synthes Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius Plate System). Orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2093-2014·2014-07-30

    Salter Labs Recalls Oxygen Masks Due to Incorrect Labeling

    Salter Labs is recalling 584 units of Model No. 8120-7 oxygen masks because the insert label incorrectly identifies the device as a non-rebreather instead of a partial rebreather.

    Product
    Oxygen Mask, Model No. 8120-7 Product Usage: Oxygen Mask, High Concentration partial rebreather, with 7 foot (2.1 m) supply tube, Elastic Strap Fixation, Single patient use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1451-2014·2014-07-30

    Shamrock Medical Recalls Docusate Calcium Softgels Due to Labeling Error

    Shamrock Medical Solutions is recalling Docusate Calcium Softgel Capsules because they were mislabeled as Docusate Sodium. The error involves a label mix-up for the specific active ingredient.

    Product
    Docusate Calcium Softgel Capsules, 240 mg, OTC, packaged and labeled to contain Docusate Sodium 240mg, Repackaged By: Shamrock Medical Solutions Lewis Center, Ohio, Mfg: Major Pharmaceuticals, Livonia, MI NDC 00904-5779-60
    Category
    Drug
    Distribution
    5 states
  • LowFDA (Food)·F-2201-2014·2014-07-30

    Dolci Gelati Recalls Sea Salt Caramel Gelato for Organic Mislabeling

    Dolci Gelati LLC is recalling YES Sea Salt Caramel Gelato because it was mislabeled as organic. The product was sold exclusively at Yes Organic Market in the MD/DC area.

    Product
    YES Sea Salt Caramel Gelato
    Category
    Food
    Distribution
    2 states
  • LowFDA (Devices)·Z-2090-2014·2014-07-30

    Zoll Circulation Recalls AutoPulse Accessories Due to Japanese Label Typo

    Zoll Circulation is recalling 161 NiMH batteries and 40 LifeBand packs distributed in Japan due to a typographical error on the Japanese legal label.

    Product
    Zoll Circulation LifeBand Single Pack (accessory), and Nickel-metal hydride (NIMH) Battery. The LifeBand is a chest compression assembly that consists of a cover plate and two bands integrated with a compression pad with a Velcro fastener. The AutoPulse Battery is a removable c
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Drugs)·D-1444-2014·2014-07-30

    X-Gen Recalls Clonidine HCl Injection Due to Labeling Error

    X-Gen Pharmaceuticals is recalling Clonidine HCl Injection vials because the side label incorrectly states the drug strength.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2200-2014·2014-07-30

    Dolci Gelati Recalls YES Green Tea Gelato for Organic Mislabeling

    Dolci Gelati LLC is recalling YES Green Tea Gelato because it was mislabeled as organic. The product was sold exclusively at Yes Organic Market in the MD/DC area.

    Product
    YES Green Tea Gelato
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-2185-2014·2014-07-23

    Zing Dark Chocolate Hazelnut Bars Recalled for Undeclared Milk

    NW Nutritional Foods LLC is recalling Zing Dark Chocolate Hazelnut bars because they contain undeclared milk despite being labeled as dairy-free or vegan.

    Product
    There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing Complete Nutrition, DARK CHOCOLATE HAZELNUT, Gluten, Soy & Dairy Free, NET WT. 1.76 OZ. (50g), Manufactured For: Zing Bars Seattle, WA 98125. Label #1 Displa
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-2187-2014·2014-07-23

    Zing Nutrition Bars Recalled for Undeclared Milk in Vegan Products

    NW Nutritional Foods LLC is recalling Zing Nutrition Bars labeled as vegan or dairy-free because they contain undeclared milk.

    Product
    There are three different labels for this product. Label #1 individual bar 100% Natural Zing Nutrition Bar, DARK CHOCOLATE SUNFLOWER MINT, Gluten Free & Vegan, NET WT. 1.76 OZ. (50g), Manufactured For: Zing Bars Seattle, WA 98125. Label #1 display Carton 100% Natural Zi
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-2186-2014·2014-07-23

    Zing Nutrition Bars Recalled for Undeclared Milk

    NW Nutritional Foods LLC is recalling Zing Nutrition Bars because they contain undeclared milk despite being labeled as dairy-free or vegan.

    Product
    There are two different labels for this product same UPC codes. Version #1 individual bars: 100% natural Zing Complete Nutrition, CHOCOLATE COCONUT, Gluten, Soy & Dairy Free, NET WT. 1.76 OZ. (50g). Version # 1 display carton: Zing Complete Nutrition, Gluten, Soy & Dair
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-2188-2014·2014-07-23

    Zing Nutrition Bars Recalled for Undeclared Milk

    NW Nutritional Foods LLC is recalling Zing Nutrition Bars labeled 'dairy free' because they contain undeclared milk.

    Product
    Individual Bars: 100% Natural Zing Nutrition Bar, CASHEW CRANBERRY ORANGE, Gluten, Dairy & GMO Free, NET WT. 1.76 OZ (50g), Manufactured For: Zing Bars Seattle, WA 98125. Display Carton: Zing Complete Nutrition, Gluten, Soy & Dairy Free, 100% natural CASHEW CRANBERRY ORANGE,
    Category
    Food
    Distribution
    46 states
  • HighFDA (Food)·F-2191-2014·2014-07-23

    Nestle Recalls Häagen-Dazs Ice Cream Due to Peanut Mislabeling

    Nestle is recalling Häagen-Dazs Chocolate Chocolate Chip Ice Cream because the ingredient label fails to identify peanuts, posing a risk to consumers with peanut allergies.

    Product
    H¿agen-Dazs Chocolate Chocolate Chip Ice Cream, 14 oz, UPC of 74570-08400
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-2071-2014·2014-07-23

    Siemens RAPIDComm Data Management System Recalled for Incorrect Test Names

    Siemens Healthcare Diagnostics Inc is recalling six RAPIDComm Data Management Systems because the 5.0 screen layout displays incorrect test names.

    Product
    Siemens RAPIDComm¿ Data Management System. The RAPIDComm¿ Data Management System manages the process of sending and receiving data from Siemens POC devices and hospital systems located in the hospital network,
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2072-2014·2014-07-23

    Integra Recalls Camino ICP Catheters for MRI Safety Labeling

    Integra LifeSciences is recalling Camino Intracranial Pressure Monitoring Kits to update labeling indicating they are unsafe in MR environments.

    Product
    Integra Camino 110-4 Intracranial Pressure (ICP) Monitoring Catheters, Cat. No's. 110-4B, 110-4G, 110-4H, 110-4L
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2078-2014·2014-07-23

    Dental EZ Group Recalls 45 Mislabelled Titan T 5K Dental Motors

    Dental EZ Group is recalling 45 Titan T 5K dental motors because the housing was incorrectly laser marked as a 20K motor.

    Product
    Titan T 5K Motor Product Usage: Low-speed motor is used with various attachments to perform a variety of dental procedures including caries removal, finishing, polishing, pin setting and prophy.The motor has a speed range of 100 to 5000 rpm capability.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Food)·F-2184-2014·2014-07-23

    Mt. Olive Jalapeno Slices Recalled for Undeclared Sulfites

    Mt. Olive Pickle Company is recalling PepperPAK Jalapeno Slices due to undeclared sulfites. The product was distributed in Florida and New York.

    Product
    Mt. Olive, PepperPAK Jalapeno Slices, 4-3.7fl oz cups, Net fl oz 14.8 (438 ml), Mt Olive Pickled Co., Inc., Corner of Cucumber and Vine, P.O. Box 609, Mt. Olive, NC 28365-0609.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2067-2014·2014-07-23

    Innovasis Recalls Excella II Pedicle Screws Due to Mislabeling

    Innovasis is recalling 32 units of Excella II Standard Pedicle Screws because the size and catalog number are mislabeled.

    Product
    Excella II Standard Pedicle Screw, Catalog No. E2S47525 and E2S47535, 4.75 mm x 25 mm. For spinal fixation. Packaged in heat-sealed plastic bag. Also provided in reusable steam sterilization tray as implant set.
    Category
    Medical Device
    Distribution
    Distributed nationwide