The Recall Desk

Hazard

Mis Labeling recalls

1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

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.

101–125 of 1381

  • HighFDA (Devices)·Z-0937-2026·2025-12-24

    Surgical Navigation Guide Contains Incorrect Instrument Compatibility Information

    SeaSpine Orthofix recalls NorthStar OCT Navigation Surgical Technique Guides due to incorrect identification of compatible Medtronic toolcards; only Solera toolcards are compatible, not Infinity toolcards.

    Product
    Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-4001
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Devices)·Z-0953-2026·2025-12-24

    Rocket 18Fg Seldinger Catheter safety guard labeling contains misleading statements causing improper securing

    Rocket Medical Plc is recalling the Rocket 18Fg Seldinger Catheter with Safety Guard due to misleading labeling that may result in improper securing and device displacement during use.

    Product
    Brand Name: Rocket Product Name: Rocket 18Fg Seldinger Catheter with Safety Guard Model/Catalog Number: R54544-18-SG Software Version: N/A Product Description: Chest tube manufactured from PVC, with fenestrations and a barium stripe to the indicated French gauge size. Supplie
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·H-0303-2026·2025-12-17

    Coffee pods mislabeled as decaf contain caffeinated product

    Gimme Coffee is recalling 252 boxes of Decaf de Agua coffee pods because the inner pods are caffeinated Deep Disco pods instead. No illnesses have been reported.

    Product
    Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods Inner-packaging/pod packaging: gimme! coffee Deep Disco caffeinated coffee pods
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0897-2026·2025-12-17

    ChemoPlus Gowns Recalled for Mislabeled Expiration Date

    Cardinal Health is recalling ChemoPlus protective gowns (251,165 units) distributed nationwide and in Canada due to incorrect expiration dating on packaging. The gowns have a three-year shelf-life but are mislabeled as five years.

    Product
    ChemoPlus gowns: Product Code Product Description CT5500T ChemoPlus Full Coverage Sleeve, Universal, Medium Blue, Non-sterile; CT5502T ChemoPlus Full Coverage Gown, Closed Back, Regular/Medium, Medium Blue, Non-sterile; CT5503T ChemoPlus Full Coverage Gown, Closed Back, Large
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0893-2026·2025-12-17

    Pillar SA PTC Spacer System Recalled Due to Inconsistent Labeling Claims

    Orthofix U.S. LLC is recalling the Pillar SA PTC Spacer System due to product labeling containing claims that are not consistently present. Approximately 13,317 units were distributed worldwide.

    Product
    Brand Name: Pillar" SA PTC Spacer System Product Name: Pillar" SA PTC Spacer System Model/Catalog Number: 39-9012SP 33W X 28L X 12.5H, 7DEG PTC IMPLANT; 39-9014SP 33W X 28L X 14H, 7DEG PTC IMPLANT; 39-9016SP 33W X 28L X 16H, 7DEG PTC IMPLANT; 39-9018SP 33W X 28L X 18H, 7DEG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0238-2026·2025-12-17

    Shloimy's Heimishe Matjes Herring Recalled for Undeclared Red Food Dye

    Kosher First LLC is recalling Shloimy's Heimishe Matjes Herring because the product contains undeclared FD&C Red #40 dye. Affected units include batch code 0103 distributed in New York.

    Product
    Shloimy's Heimishe Matjes Herring packaged in 7oz plastic container
    Category
    Food
    Distribution
    0 states
  • LowFDA (Drugs)·D-0223-2026·2025-12-17

    Morphine sulfate oral solution recalled due to carton label size mismatch

    Winder Laboratories is recalling 3,528 bottles of morphine sulfate oral solution because the carton label states an incorrect bottle size that does not match the actual bottle inside.

    Product
    MORPHINE SULFATE — MORPHINE SULFATE (MORPHINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0895-2026·2025-12-17

    Forza Ti Spacer System Recalled for Labeling Inconsistencies

    Orthofix U.S. LLC is recalling 14,201 units of the Forza Ti Spacer System, a spinal fusion device, due to labeling inconsistencies where claims are not consistently present across affected units.

    Product
    Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 7H; 38-2008SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 8H; 38-2009SP F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0302-2026·2025-12-10

    Protein Powder Recalled for Undeclared Milk Allergen and Incorrect Labeling

    Genepro Whey 4th Generation Plasma Treated Protein is recalled for mislabeling containing incorrect ingredient information and failing to declare milk as an allergen.

    Product
    Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable mylar bag, UPC 850053365126, Manufactured For: Genepro Protein, Inc. 15000 Weston Parkway, Cary NC 27513 Front label reads, in part: "* LACTOSE FREE * DAIRY FREE *
    Category
    Food
    Distribution
    37 states
  • ModerateFDA (Food)·H-0233-2026·2025-12-10

    Prenatal Vitamin Recalled for Undeclared Soy and Labeling Error

    Avion Pharmaceuticals is recalling 804 bottles of Prenate Chewable prenatal vitamin due to undeclared soy not listed on the label and incorrect boron dosage labeling (250mg instead of 250mcg per serving).

    Product
    Prenate Chewable¿ A chewable Rx prenatal vitamin with a delicious chocolate flavor with Quatrefolic Dietary Supplement 30 Tablets Rx Only UPC 3 75854 30630 2 Manufactured for: Avion Pharmaceuticals, LLC Alpharetta, GA 30005
    Category
    Food
    Distribution
    17 states
  • ModerateFDA (Devices)·Z-0876-2026·2025-12-10

    KWIK-STIK Quality Control Kit Packaging Labeling Error Recall

    Microbiologics Inc is recalling KWIK-STIK quality control kits due to labeling errors. Some units from lot 818-111-7 were packaged in containers labeled with an incorrect lot number.

    Product
    KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0214-2026·2025-12-10

    Haloperidol Lactate Injection Recalled for Incorrect RFID Tags

    Safecor Health recalled Haloperidol Lactate Injection due to incorrect RFID tag serial numbers applied during repackaging. The error affects 800 vials distributed in Massachusetts.

    Product
    HALOPERIDOL LACTATE — HALOPERIDOL LACTATE (HALOPERIDOL LACTATE)
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0600-2026·2025-12-03

    Medical Device Illumination Pack Recalled for Undisclosed Latex in Packaging

    Stryker Corporation is recalling the NICO Myriad Illumination Pack because tape used in packaging contains latex despite the product being labeled as latex-free. Latex may cause allergic reactions in sensitive individuals.

    Product
    NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0599-2026·2025-12-03

    NICO Myriad Surgical Handpieces Recalled for Latex Contamination in Packaging

    Stryker has recalled NICO Myriad surgical handpieces because packaging tape contains latex despite products being labeled latex-free. Latex exposure could cause allergic reactions in sensitive patients.

    Product
    NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0584-2026·2025-12-03

    Blood Lead Test System Recalled Due to Mislabeled Calibration Buttons

    Magellan Diagnostics is recalling the LeadCare II Blood Lead Test Kit due to mislabeled calibration buttons that could produce inaccurate test results. Approximately 1,774 units distributed nationwide may give falsely elevated or falsely low lead readings.

    Product
    The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0596-2026·2025-12-03

    FlexLab Aliquoter Module May Generate Unlabeled Sample Tubes

    The FlexLab's Aliquoter Module may produce sample tubes without labels or with mismatched labels, potentially causing delayed or incorrect lab results if operators don't properly clear the printer buffer during maintenance.

    Product
    FlexLab (FLX); Version: FLX-217-40;
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0180-2026·2025-11-26

    Potassium Chloride Injection Recalled for Incorrect Strength on Overwrap Label

    A Potassium Chloride prescription injection has been recalled due to a labeling error on the overwrap. The label may incorrectly identify the product as 10 mEq instead of 20 mEq.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0181-2026·2025-11-26

    Potassium Chloride Injection Recalled Nationwide for Mislabeled Strength

    Potassium chloride injectable medication is being recalled due to overwrap labels incorrectly stating strength as 10 mEq instead of 20 mEq. This error could result in incorrect dosing by healthcare providers.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0540-2026·2025-11-26

    Tribio Implant Recalled for Incorrect Product Name on Outer Packaging

    Berkeley Advanced Biomaterials is recalling Tribio Implant 7.5mm x 40mm units due to incorrect product name printed on the outer packaging. The recall affects 62 units distributed in Tennessee.

    Product
    Tribio Implant 7.5mm x 40mm REF M80 SB008 UDI code: (01) 00816125023653(10) EBL10B13C(17) 270630 Tribio" Implant is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0179-2026·2025-11-19

    Food candy bar recalled for undeclared peanut allergen

    Zingerman's Ca$hew Cow Candy Bar (Lot #174250) was recalled due to undeclared peanut. The product was distributed to retailers in Michigan and New York.

    Product
    Zingerman's Ca$hew Cow Candy Bar net wt 2oz UPC 844397000157
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-0314-2026·2025-11-12

    Osstem Dental X-Ray System T2 Missing Regulatory Certification Statement

    OSSTEM Implant Co. is voluntarily recalling Osstem Dental X-Ray System T2 devices due to missing required FDA certification statements on their labeling.

    Product
    Osstem Dental X-Ray System T2. Product Model Numbers T2-C and T2-CS.
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-0313-2026·2025-11-12

    Osstem Dental X-Ray Systems Recalled for Missing Regulatory Certification Statement

    OSSTEM Implant Co., Ltd. is voluntarily correcting labeling for Osstem Dental X-Ray System T1 models T1-C and T1-CS because their labels may be missing a required FDA certification statement confirming compliance with radiological health standards.

    Product
    Osstem Dental X-Ray System T1. Product Model Numbers T1-C and T1-CS.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·24V548000·2025-11-07

    Multiple Toyota models recalled for incorrect load capacity labels

    Gulf States Toyota is recalling multiple 2023-2025 Toyota models with inaccurate load carrying capacity labels that may cause overloading and crash risk. Owner notification was sent in September 2024 and replacement labels will be mailed at no charge.

    Product
    TOYOTA — 2024 TOYOTA TACOMA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0136-2026·2025-11-05

    Weaver Nut Company Recalls Chocolate Nonpareils for Undeclared Milk Allergen

    Weaver Nut Company recalls D2645 chocolate nonpareils due to undeclared milk allergen. The product was distributed across 14 states.

    Product
    D2645 - Nonpareils, Semi-Sweet Chocolate (White Seeds), 25lb Bulk Cases Packaged into Various Size Units After distribution.
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-0229-2026·2025-10-29

    Surgical Screw Packaging Mislabeled With Incorrect Length

    Synthes locking screws used in femoral and tibial nailing systems were packaged with incorrect length labels: 42mm screws marked as 46mm and 46mm screws marked as 42mm. The correct length is etched on each screw.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 42MM / XL25/ STER. Product Code: 04.045.342TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide