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.

2951–2975 of 9607

  • HighNHTSA·19V191000·2019-03-08

    Forest River Surveyor Recalled for Incorrect Axle Weight Placard

    Forest River is recalling 2018-2019 Surveyor trailers because the Federal Placard lists 3,500 lb axles instead of the actual 2,500 lb capacity, risking overload and loss of control.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1057-2019·2019-03-06

    Puratos Tegral Satin Gold CL Crème Cake Recalled for Undeclared Milk

    Puratos Corporation is recalling Tegral Satin Gold CL Crème Cake because the product contains undeclared milk. The recall affects 25,700 lbs distributed across nine states.

    Product
    Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1060-2019·2019-03-06

    Ottogi Ramen Bokki Cup Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling 1.6 million units of Ramen Bokki cup noodles due to an undeclared egg allergen. Consumers should stop eating the product.

    Product
    Ottogi Ramen Bokki (Cup) 4.23oz x 12ea Item #21309009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighNHTSA·19V168000·2019-03-06

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Incorrect Weight Label

    Highland Ridge RV is recalling 74 units of 2019 Mesa Ridge and Open Range Ultra Lite travel trailers because the weight label exceeds the safety chain rating.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1064-2019·2019-03-06

    Ottogi Jjajang Bokki Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Jjajang Bokki noodle bowls because they contain egg, which is not listed on the label.

    Product
    Ottogi Jjajang Bokki (Bowl) 4.23oz x 12ea Item #21502157 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1063-2019·2019-03-06

    Ottogi Snack Ramen Recalled for Undeclared Egg Allergen

    Ottogi America is recalling specific lots of Ottogi Snack Ramen cups because they contain egg, which is not listed on the label.

    Product
    Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1074-2019·2019-03-06

    Ottogi Spicy Seafood Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Jin Jjambbong Spicy Seafood Noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi Jin Jjambbong Spicy Seafood Noodle 4.58 oz x 4 ea Item #32142443 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1058-2019·2019-03-06

    Ottogi Ramen Sari Recalled for Undeclared Egg Allergen

    Ottogi America is recalling 1.6 million units of Ramen Sari noodles due to an undeclared egg allergen. The product was distributed in 12 U.S. states and Canada.

    Product
    Ottogi Ramen Sari (Extra Noodle) 3.88oz x 48ea Item #21101009 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1137-2019·2019-03-06

    Gilda Industries Recalls Butter Pound Cake for Undeclared Milk Allergen

    Gilda Industries is recalling Panque Butter Pound Cake because the product fails to declare milk as an ingredient. The recall covers specific lots distributed to domestic consignees.

    Product
    Gilda Industries, Panque - Butter Pound Cake, Manufactured by and Distributed for Gilda Industries
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1069-2019·2019-03-06

    Ottogi Ppushu Ppushu Spicy Flavor Noodles Recalled for Undeclared Egg

    Ottogi America is recalling Ppushu Ppushu Spicy Flavor noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi Ppushu Ppushu Spicy Flavor 3.17oz x 40ea Item #21503008 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-1059-2019·2019-03-06

    Ottogi Yeul Ramen Bowl Recall for Undeclared Egg Allergen

    Ottogi America is recalling 1,594,338 units of Ottogi Yeul Ramen (Bowl) because the product contains egg, which is not declared on the label.

    Product
    Ottogi Yeul Ramen (Bowl) 4.06oz x 12ea Item #21305007 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0966-2019·2019-03-06

    Terumo Cardiovascular Procedure Kit Recalled for Undeclared Natural Rubber Latex

    Terumo Cardiovascular Systems Corporation is recalling 12 packs of Cardiovascular Procedure Kits because the presence of natural rubber latex is not declared on the label.

    Product
    Cardiovascular Procedure Kit (CLR MP4 COIL 2 SPIKE) Catalog Number: 140222
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0960-2019·2019-03-06

    Abbott Vascular Recalls PLUS 30 Priority Pack Accessory Kit Due to Expiration Error

    Abbott Vascular is recalling 26 units of the PLUS 30 Priority Pack Accessory Kit because an incorrect expiration date was entered for one lot.

    Product
    PLUS 30 PRIORITY PACK Accessory Kit Product Usage: Is recommended for use during vascular procedures in conjunction with interventional and / or diagnostic devices (e.g., balloon dilatation catheters, atherectomy devices, stent delivery systems, intravascular ultrasound devic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1101-2019·2019-03-06

    Klaire Labs Melatonin Lozenge Formula Recalled Due to Incorrect Ingredient

    ProThera, Inc. is recalling 120 bottles of Klaire Labs Melatonin Lozenge Formula because the product was filled with L-Theanine instead of melatonin.

    Product
    Klaire Labs Melatonin Lozenge Formula Fast Dissolving 1 mg tablets; Packed in a 75 cc HDPE Bottle 60 Tablets UPC: 8 28054 17845 8; SKU: ML1
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-1054-2019·2019-03-06

    King Orchards Tart Cherry Concentrate Recalled for Incorrect Sugar Labeling

    King Orchards is recalling Montmorency Tart Cherry Concentrate because the nutrition label lists 1g of sugar per serving instead of the actual 15g.

    Product
    Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold individual and 12 per case), and 1-oz packet (sold individual and per 25, 50, 100, 250, 300, and 1000)
    Category
    Food
    Distribution
    20 states
  • ModerateFDA (Food)·F-1097-2019·2019-03-06

    Planetary Herbals Mullein Lung Complex Recalled for Labeling Error

    Planetary Herbals is recalling Mullein Lung Complex capsules due to a labeling error regarding inactive ingredients.

    Product
    Planetary Herbals Mullein Lung Complex; 1000 mg; 15 count, item number PF0003; 90 count - Item number PF0002; 180 count, Item number PF0106 and 90 + 90 count, PF 7013 white plastic bottles. Proprietary Blend: Platycodon root, Ophiopagon Rhizome, Long Pepper Fruit, Black Cher
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0963-2019·2019-03-06

    BrosMed Hermes NC PTA Balloon Catheter Recalled for Labeling Error

    BrosMed Medical Co., Ltd. is recalling 400 Hermes NC PTA Balloon Dilatation Catheters because the labels display incorrect, higher-rated burst pressure information.

    Product
    Hermes NC PTA Balloon Dilatation Catheter The balloon dilatation catheter is intended to dilate stenoses in the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysi
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0938-2019·2019-03-06

    Zimmer Biomet Recalls Vanguard Knee Patella Implants Due to Labeling Mismatch

    Zimmer Biomet is recalling 90 Vanguard Knee System patella implants because a potential commingle could result in the implant size not matching the label.

    Product
    Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766
    Category
    Medical Device
    Distribution
    2 states
  • LowFDA (Devices)·Z-0958-2019·2019-03-06

    Exactech Equinoxe Humeral Stem Recalled for Incorrect Packaging Instructions

    Exactech is recalling 40 Equinoxe Preserve Humeral Stems because they may have been packaged with instructions for a different knee implant.

    Product
    Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally mature individuals with degenerative diseases of the glenohumeral joint where anatomic total arthroplasty,anatomic hemi-arthroplasty,or reverse total arthroplast
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V171000·2019-03-05

    2019 Western Star Trucks Recalled for Odometer Unit Labeling Error

    Daimler Trucks North America is recalling 2019 Western Star 4700 and 4900 trucks because the odometer displays miles but tracks kilometers, potentially causing driver confusion.

    Product
    WESTERN STAR — WESTERN STAR 4700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0848-2019·2019-02-27

    Ortho-Clinical Diagnostics Recalls VITROS VALP Reagent Packs Due to Negative Bias

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products VALP Reagent Packs because they may produce negative bias results when measuring valproic acid.

    Product
    VITROS Chemistry Products VALP Reagent Pack. For in vitro diagnostic use only. CATALOG #(s): 6801710 INTENDED USE: For in vitro diagnostic use only. VITROS Chemistry Products VALP Reagent is used on the VITROS 5,1 FS Chemistry System, the VITROS 4600 Chemistry System and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0852-2019·2019-02-27

    Boston Scientific Recalls Mislabelled Stingray Guidewires for Coronary Procedures

    Boston Scientific is recalling 49 Stingray Guidewires that are 185cm but incorrectly labeled as 300cm. The mislabeling could lead to improper use during angioplasty procedures.

    Product
    Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other intravascular devices during percutaneous transluminal coronary angioplasty (PTCA) and percutaneous transluminal angioplasty (PTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0938-2019·2019-02-27

    Century Snacks Recalls Praline Pecans Due to Mispackaging

    Century Snacks LLC is recalling 25 packages of Praline Pecans because they were mispackaged with Praline Almonds. The error creates an undeclared allergen risk for consumers with nut allergies.

    Product
    Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040 centurysnacks.com
    Category
    Food
    Distribution
    6 states