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.

1526–1550 of 9607

  • HighFDA (Food)·F-0388-2021·2021-04-14

    B&G Sweet Heat Pepper Dip Recalled for Undeclared Milk Allergen

    B&G Sweet Heat Peppers is recalling 43 cases of Sweet Heat Pepper Dip because the label fails to declare milk, despite containing cream cheese and sour cream.

    Product
    B&G Sweet Heat Pepper Dip, Ready To Eat, Refrigerated, packaged in 10 oz, semi-rigid plastic container. UPC 7 42832 07566 4. Product label is read in parts: "***SWEET HEAT PEPPER DIP ***Ingredients: Cream Cheese, Sour Cream, Jalapenos, Sugar, Apple Cider Vinegar, Granulated Garl
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0424-2021·2021-04-14

    Babco Foods Recalls Anand Far Far Garlic Sandige for Undeclared Yellow 6

    Babco Foods International is recalling Anand Far Far (Garlic Sandige) because it contains undeclared Yellow 6, a food dye.

    Product
    Anand Far Far (Garlic Sandige) Net Weight 7 oz./200 g package ingredients: rice, wheat flour, garlic, red chilli, refined palm oil and salt. UPC 8 78776 00232 6 Product of India Imported and Distributed by Babco Foods International, LLC, Bridgewater, NJ
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1352-2021·2021-04-14

    Clerio Vision Recalls Extreme H2O 59% Contact Lenses for Mislabeled Power

    Clerio Vision is recalling 153 Extreme H2O 59% contact lenses because they may be mislabeled with the incorrect lens power.

    Product
    EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit astigmatism
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0385-2021·2021-04-14

    New Generation Wellness Recalls Vegan Vitamin D3 Tablets for Stability Issues

    New Generation Wellness Inc. is recalling 2,330 bottles of Vegan Vitamin D3 tablets because stability samples showed potency below the label claim.

    Product
    VEGAN VITAMIN D3, 50 mcg (2,000 IU), 60 VEGAN TABLETS in 100cc amber glass bottles. UPC 7 19985 61831 4; UPC 6 10265 58337 0; UPC 4 01008 61831 8; UPC 4 02008 61831 5. Store in a cool, dry place. Product is sold under 72 private labels: A Moveable Feast; Akin's Natural Foods;
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1354-2021·2021-04-14

    Integra LifeSciences Recalls CODMAN HAKIM BACTISEAL Shunt Catheters Due to Labeling Error

    Integra LifeSciences is recalling 49 units of CODMAN HAKIM BACTISEAL Shunt System catheters because they lacked required drainage holes and markings.

    Product
    CODMAN HAKIM BACTISEAL Shunt System Clear with Barium Stripe Peritoneal Catheter 120cm, with drainage Holes and Marking. For use in the treatment of hydrocephalus. Catalog Number: NS5524
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Drugs)·D-0319-2021·2021-04-14

    Kimberly-Clark Recalls Scott Moisturizing Foam Hand Sanitizer Due to Labeling Error

    Kimberly-Clark is recalling Scott Moisturizing Foam Hand Sanitizer because some bottles containing Foam Skin Cleanser soap are incorrectly labeled as hand sanitizer.

    Product
    Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199 Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5 UPC 0 36000 91592 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1351-2021·2021-04-14

    Nuvasive Freedom End Caps Recalled for Missing Biological Assessments

    Nuvasive Specialized Orthopedics Inc. is recalling 59 units of Freedom End Caps and related components because they lack full biological assessments and are not indicated for patients under 18.

    Product
    NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged End Cap 8.5/10.7mm,¿ +0mm; Packaged End Cap 8.5/10.7mm,¿ +5mm; Packaged End Cap 8.5/10.7mm,¿ +10mm; Packaged End Cap 8.5/10.7mm,¿ +15mm; Packaged End Cap 8.5/10.7mm,¿ +20mm; Pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0384-2021·2021-04-14

    CVS Live Better Vitamin D3 Recalled for Stability Issues

    New Generation Wellness Inc. is recalling Live Better vegan vitamin D-3 tablets because stability samples showed less than 100% of the label claim.

    Product
    Live Better vegan vitamin d-3 by CVS Health, 50 mcg (2000 IU), 40 tablets in blue PET jar, Distributed by: CVS Pharmacy, Inc. one CVS Drive, Woonsocket, RI 02895, UPC 0 50428 62499 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0322-2021·2021-04-14

    Washington Homeopathic Products Recalls Sp-4 Solution Due to Ingredient Error

    Washington Homeopathic Products, Inc. is recalling 114 bottles of Sp-4 solution because the product was manufactured with Potassium Chloride instead of Potassium Phosphate.

    Product
    Sp-4, 100 mL solution bottles, Rx only, Washington Homeopathic Products, Inc.260 J R Hawvermale Way Berkeley Springs West Virginia 25411
    Category
    Drug
    Distribution
    3 states
  • HighFDA (Devices)·Z-1317-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 100 units of DiamondTemp Unidirectional Small Curve Ablation Catheters because packaging and instructions list incorrect catheter sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF CEDT100S, SterileEO, UDI 00812499030198
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1322-2021·2021-04-07

    EPIX Therapeutics DiamondTemp Catheter Recalled for Labeling Errors

    EPIX Therapeutics is recalling 13 DiamondTemp Unidirectional Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Large Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT200L, SterileEO, Rx Only, UDI: 00812499030013
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1319-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 15 DiamondTemp Bidirectional Small Curve Ablation Catheters because the packaging and instructions for use list incorrect catheter sizes.

    Product
    EPIX Therapeutics DiamondTemp Bidrectional Small Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB300S, SterileEO, UDI: 00812499030358
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1321-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 19 DiamondTemp Unidirectional Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Ablation Catheter, Small Curve, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:DT100S,SterileEO, Rx Only, UDI: 00812499030006
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1320-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 18 units of DiamondTemp Bidirectional Large Curve Ablation Catheters because packaging and instructions list incorrect sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Bidrectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF:CEDTB400L, SterileEO, UDI: 00812499030303
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1318-2021·2021-04-07

    EPIX Therapeutics Recalls DiamondTemp Ablation Catheters Due to Labeling Errors

    EPIX Therapeutics is recalling 60 units of DiamondTemp Unidirectional Large Curve Ablation Catheters because packaging and instructions list incorrect catheter sizes, posing a risk of blood clots or air emboli.

    Product
    EPIX Therapeutics DiamondTemp Unidirectional Large Curve Ablation Catheter, 7.5 French Size(2.48 mm), Connector Type: ODU 19 PIN, REF: CEDT200L, Sterile EO, UDI: 00812499030259
    Category
    Medical Device
    Distribution
    0 states
  • LowFDA (Devices)·Z-1310-2021·2021-04-07

    Arthrex Recalls Cannulated Drill Bits Due to Incorrect Color Indicator

    Arthrex, Inc. is recalling 9 units of 5.0 mm cannulated drill bits because the color indicator on the shaft is the incorrect color.

    Product
    Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowNHTSA·21V237000·2021-04-05

    Mercedes-Benz Sprinter VIN Mismatch Recall

    Daimler Vans USA is recalling one 2019 Mercedes-Benz Sprinter because its VIN numbers do not match, potentially preventing owners from receiving safety recall notices.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0351-2021·2021-03-31

    Taylor Farms Recalls Tuna Salad Croissant Sandwiches for Undeclared Soy

    Taylor Farms Northwest is recalling 577 units of Tuna Salad Croissant Sandwiches because the product contains soy lecithin that is not declared on the label.

    Product
    Item #140952, Tuna Salad Croissant Sandwich, Refrigerated, packaged in clear plastic clamshell container. Ready to Eat product sold in foodservice, retail, and deli stores. Net wt. 7.8 OZ (221g). UPC 0 30223 11097 2. The label is read in parts: "***CHICKEN SALAD Croissant***
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0352-2021·2021-03-31

    Buc-ee's Butter Toffee Almonds Recalled for Peanut Mislabeling

    Lehi Valley Trading Co is recalling Buc-ee's Butter Toffee Almonds because the product contains peanuts but is labeled as almonds.

    Product
    Buc-ee's Butter Toffee Almonds, 12 oz., packaged in clear zip top bag with stickered label, UPC: 0 9524842002 4, Manufactured and packaged at Lehi Valley Trading Company 4955 . McKellips Rd, Mesa, AZ 85215. branded and statement on label "Distributed by Buc-ee's LTD. 327 FM 2004
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0350-2021·2021-03-31

    Taylor Farms Recalls Chicken Salad Croissant Sandwiches for Undeclared Soy

    Taylor Farms Northwest is recalling Chicken Salad Croissant Sandwiches because the product contains soy lecithin that is not declared on the label.

    Product
    Item #140946, Chicken Salad Croissant Sandwich, Refrigerated, packaged in clear plastic clamshell container. Ready to Eat product sold in foodservice, retail, and deli stores. Net wt. 7.8 OZ (221g). UPC 0 30223 11099 6. The label is read in parts: "***CHICKEN SALAD CROISSANT
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1290-2021·2021-03-31

    Corin Trinity Hip Prosthesis Heads Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of Trinity Biolox Delta Ceramic Heads due to incorrect size labeling on packaging and patient stickers.

    Product
    Corin BIOLOX DELTA MOD HEAD 32mm EX LONG +7mm 12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit, titani
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2021·2021-03-31

    Corin Trinity Acetabular System Recalled for Incorrect Size Labeling

    Corin Ltd is recalling 23 units of the Trinity Acetabular System because the size indicated on the packaging and patient stickers is incorrect.

    Product
    Corin BIOLOX DELTA MOD HEAD 36mm EX LONG +8mm12/14 TAPER. Corin Trinity Acetabular System with Extra Long Heads/Trinity Biolox Delta Ceramic Head (Generic Name: Hip Prosthesis). The Trinity Acetabular System is a modular acetabular cup system consisting of a press fit, titanium
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V218000·2021-03-29

    Winnebago Recalls 2020 Minnie RVs Due to Incorrect Tire Labeling

    Winnebago is recalling 2020 Minnie vehicles because the Tire and Loading Information label lists the wrong tire size, which could lead to improper tire installation and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1262-2021·2021-03-24

    Merit Medical Recalls HeartSpan Transseptal Needles Due to Tip Curvature Mismatch

    Merit Medical Systems is recalling 587 HeartSpan Transseptal Needles because the labeled tip curvature may not match the actual curvature, posing a risk of unintended anatomy puncture.

    Product
    HeartSpan Transseptal Needles Catalog No. FND-019-01, Lot No. E1913644 consisting of an outer needle cannula and an inner stylet. The needle is comprised of flexible thin walled tubing with an ergonomic hub and stopcock attached to the proximal end. The stylet consists of a soli
    Category
    Medical Device
    Distribution
    18 states
  • SevereFDA (Devices)·Z-1263-2021·2021-03-24

    Heartspan Transseptal Needle Recall Due to Tip Curvature Mismatch

    Merit Medical Systems is recalling Heartspan Transseptal Needles because the labeled tip curvature may not match the actual curvature, posing a risk of unintended anatomy puncture.

    Product
    Heartspan Transseptal Needles, Catalog No. FND-019-02, Lot No. E1913645 consisting of an outer needle cannula and an inner stylet. The needle is comprised of flexible thin walled tubing with an ergonomic hub and stopcock attached to the proximal end. The stylet consists of a soli
    Category
    Medical Device
    Distribution
    18 states