The Recall Desk

Hazard

Mis Labeling recalls

9,610 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,610
Critical
161
Severe
588
Most recent
2026-09-16

Of the 9,610 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 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.

5226–5250 of 9610

  • ModerateFDA (Food)·F-0146-2017·2016-10-26

    Fresh Express American Salad Recalled for Incorrect Condiment Kits

    Fresh Express is recalling American Salad bags that may contain incorrect condiment kits. Consumers in six states should check their products.

    Product
    Fresh Express American Salad, 11 oz., Product Code G264A12B, Use-By Date OCT 05
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0289-2017·2016-10-26

    US Endoscopy Recalls Vari-Safe Injection Needles Due to Incorrect Distribution

    US Endoscopy is voluntarily recalling one lot of Vari-Safe Injection Needles because the lot was incorrectly distributed with different internal catheter components.

    Product
    Vari-Safe Injection Needle US endoscopy 5976 Heisley Road Mentor, Ohio 44060 A sterile, single use, flexible sheath device intended to be used for the injection of various types of media through flexible endoscopes
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Food)·F-0188-2017·2016-10-26

    King Henry's Gummy Frogs Recalled for Undeclared Colors

    King Henry's is recalling Gummy Frogs because they may contain undeclared food dyes. Consumers should stop eating the product.

    Product
    Gummy Frogs, 6oz, UPC 6105465200, 61054645500
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0090-2017·2016-10-26

    Ortho-Clinical VITROS Chemistry LAC Slides Recalled Due to NAC Interference

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry LAC Slides because N-Acetylcysteine (NAC) can interfere with the assay results.

    Product
    VITROS Chemistry Products LAC Slides, REF/Product Codes 843 3880 (300 slides per sales unit) and 815 0112 (90 slides per sales unit), Unique Device Identifier Nos. 10758750004911 and 10758750004454, Rx ONLY, IVD --- For in vitro diagnostic use only. VITROS Chemistry Products L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0111-2017·2016-10-26

    Zimmer Biomet Recalls Vanguard Distal Femoral Augments Due to Labeling Error

    Zimmer Biomet is recalling five Vanguard Distal Femoral Augments because the product inside the carton does not match the label. The mismatched size is easily identified during surgery.

    Product
    Vanguard Distal Femoral Augment 75 X 5 RL/LM Product Usage:  Painful and disabled knee joint resulting from osteoarthritis, rheumatoid arthritis, traumatic arthritis where one or more compartments are involved.  Correction of varus, valgus, or posttraumatic deformity.  Cor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0113-2017·2016-10-26

    Osteogenics Recalls Cytoplast Membrane Due to Packaging Error

    Osteogenics Biomedical, Inc. is recalling 32 boxes of Cytoplast Titanium-Reinforced Posterior Singles Membrane because the device may be packaged in the wrong product box.

    Product
    Cytoplast Titanium-Reinforced Posterior Singles Membrane A temporarily implantable material (non-resorbable) for use as a space-making barrier in the treatment of periodontal bone defects.
    Category
    Medical Device
    Distribution
    0 states
  • HighUSDA FSIS·098-2016·2016-10-21

    Brookwood Farms Recalls Pulled Pork Due To Undeclared Soy Allergen

    Brookwood Farms is recalling 126,570 pounds of pulled pork products because they contain soy, an undeclared allergen. No illnesses have been reported.

    Product
    Brookwood Farms — Brookwood Farms, Inc. Recalls Pulled Pork Products Due To Misbranding And An Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0087-2017·2016-10-19

    NatureBox Dark Cocoa Nom Noms Recalled for Undeclared Peanut Allergen

    NatureBox is recalling Dark Cocoa Nom Noms because some bags may contain peanut butter but do not list peanuts on the label.

    Product
    Dark Cocoa Nom Noms 4.5oz. (128g) UPC: 8 54557 00533 5 Lot 16083 Product is shipped directly to customers per individual order or to corporate customers in 20 x 4.5 oz. bags cases. Ingredients: Rolled Oats, Almonds. For address freshness (Grape juice, rice dextrin), hon
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0006-2017·2016-10-19

    Uncle Buck's Maple Nut Candy Recalled for Undeclared Peanut Allergen

    Rucker's Wholesale & Service Co. is recalling Uncle Buck's Maple Nut candy because the label fails to list peanuts, a major allergen, as an ingredient.

    Product
    Uncle Buck's Maple Nut candy packaged in a clear plastic 2.7 oz. bag with attached green, orange, and white label with Organe and black writing.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0007-2017·2016-10-19

    Cabela's Maple Nut Candies Recalled for Undeclared Peanut Allergen

    Rucker's Wholesale & Service Co. is recalling Cabela's Maple Nut candies because the label fails to list peanuts, a major allergen.

    Product
    Cabela's classic candies Maple nut packaged in 2.7 oz. clear plast ice bag with brown label attached with brown lettering.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2017·2016-10-19

    TheraSphere Y-90 Microspheres Recalled for Incorrect Radioactivity Labeling

    Biocompatibles U.K., Ltd. is recalling one dose of TheraSphere Y-90 Glass Microspheres shipped to Hong Kong because the labeled radioactivity was incorrect.

    Product
    TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a neoadjuvant to surgery or transplantation in patients with unresectable HCC who can have placement of appropriately positioned hepatic arterial catheters.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-0080-2017·2016-10-19

    Taylor Farms Cranberry Walnut Salad Recalled for Incorrect Allergen Labeling

    Taylor Farms is recalling Cranberry Walnut Salad kits because some packages have incorrect labels that fail to declare walnuts or wheat.

    Product
    Taylor Farms Cranberry Walnut Salad; Salad kit for one: Baby Lettuce Blend, Feta Cheese, Flat Bread Chips, Dried cranberries and Walnuts and Raspberry Vinaigrette dressing. Distributed by: Taylor Farms Inc., Salinas, CA.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0043-2017·2016-10-19

    Doctor Kracker Pumpkin Seed Cheddar Crispbreads Recalled for Undeclared Milk

    Kracker Enterprises is recalling Doctor Kracker Pumpkin Seed Cheddar Crispbreads because the ingredient statement does not list milk, despite the product name containing Cheddar.

    Product
    Doctor Kracker Pumpkin Seed Cheddar Crispbreads Net Wt. 7 oz. (200g) in cardboard container.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Food)·F-0082-2017·2016-10-19

    Chaos and Pain Recalls Cannibal Riot Pre-Workout for Undeclared Ingredients

    Chaos and Pain is recalling Cannibal Riot pre-workout supplements because they contain undeclared Agmatine and 1,3 Dimethylbutylamine, which is not permitted in the EU.

    Product
    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314669
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0069-2017·2016-10-19

    Supermom's Kitchen Roast Beef Melt Recalled for Undeclared Ingredients

    Northern Tier Bakery is recalling Supermom's Kitchen Roast Beef & Cheddar Melt because the product was mislabeled and failed to declare monosodium glutamate, yellow 5, and yellow 6.

    Product
    Supermoms Kitchen Roast Beef & Cheddar Melt, Net Wt. 3.7 oz (105g). Keep Refrigerated. UPC 63913-94236
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0063-2017·2016-10-19

    A&D Blood Pressure Monitors Recalled for Small Cuff Labeling Error

    A&D Engineering is recalling 378 blood pressure monitors that were not labeled for use with small cuffs. The devices were distributed to distributors in New York, Massachusetts, Virginia, and Texas.

    Product
    Blood Pressure Monitor UA-767PBT-Ci for small cuff. Designed to be used by end users who are eighteen (18) years and older at home to monitor their blood pressure (systolic and diastolic) and pulse rate.
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-0059-2017·2016-10-19

    Teleflex Johans Grasper Recall Due to Labeling Error

    Teleflex Medical is recalling 160 Johans Graspers because they were mislabeled as Gripper Graspers. The sterile surgical instruments were distributed to six US states.

    Product
    Teleflex Percuaneous Solutions, Johans Grasper, Ref ML004EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdom
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-0044-2017·2016-10-19

    Doctor Kracker Crispbreads Recalled for Incorrect Milk Labeling

    Kracker Enterprises is recalling Doctor Kracker Klassic 3 Seed Crispbreads because the packaging lists milk as an ingredient, even though the product does not contain milk.

    Product
    Doctor Kracker Klassic 3 Seed Crispbreads Net Wt 7 oz (200g) in cardboard container.
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-0058-2017·2016-10-19

    Teleflex Gripper Graspers Recalled for Labeling Error

    Teleflex Medical is recalling 160 Gripper Graspers due to a labeling error where they were mislabeled as Johans Graspers.

    Product
    Teleflex Percuaneous Solutions, Gripper Grasper, Ref ML003EE, Rx Only Sterile Manufactured for: Teleflex Medical, Park, NC 27709 The Percutaneous Surgical System with 5 mm attachments is indicated for the means to penetrate soft tissue to access certain areas of the human abdo
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Food)·F-0045-2017·2016-10-19

    Wegmans Organic Blush Sauce Recalled for Incorrect Milk Allergen Labeling

    LiDestri Foods is recalling Wegmans Organic Blush Sauce because jars were labeled with a cream sauce allergen declaration for milk.

    Product
    Wegmans ITALIAN CLASSICS Organic BLUSH SAUCE, NET WT 23.5 OZ (1 LB 7.5 OZ) 667g
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-0081-2017·2016-10-19

    Chaos and Pain Recalls Cannibal Riot Pre-Workout for Undeclared Ingredients

    Chaos and Pain is recalling Cannibal Riot pre-workout supplements because they contain undeclared Agmatine and 1,3 Dimethylbutylamine, which is not permitted in the EU.

    Product
    CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT. 10.5 oz (300g), UPC 610563314652
    Category
    Food
    Distribution
    0 states
  • HighNHTSA·16V751000·2016-10-18

    Forest River Surveyor Recalled for Incorrect Federal Tire Placard

    Forest River is recalling 2016-2017 Surveyor recreational vehicles because the Federal Placard lists incorrect tire and rim specifications, which could lead to over-inflation and tire failure.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2307-2016·2016-10-12

    Four Seasons Pecan Tarts Recalled for Undeclared Milk

    Charlie's Specialties, Inc. is recalling Four Seasons Pecan Tarts because they contain undeclared milk. The product was distributed in Ohio.

    Product
    Four Seasons Pecan Tarts; 202 4T0867 ; Sel By: 09/10/2016, 09/15/15, 10/13/16,10/28/16; and 12/10/15, 12/15/15, 01/13/16, 01/28/16 (lot numbers). 180 Pieces; Weight 8#; Packed exclusively for International Market Brands, Cleveland, Ohio 44146.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2606-2016·2016-10-12

    Apple Pecan Cake Recalled for Missing Pecan Allergen Labeling

    Creative Occasions, Inc. is recalling Patti's good life Premium Apple Pecan Cake because the ingredient statement failed to declare pecans.

    Product
    Patti's good life PREMIUM APPLE PECAN CAKE, NET WT 20 OZ (1 LB 4 OZ) 567g, UPC 89028800290
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Devices)·Z-2915-2016·2016-10-12

    New Star Lasers Recalls VariaBreeze Systems Due to Labeling Notification Failure

    New Star Lasers is recalling 17 VariaBreeze laser systems because customers were not notified when promotional material was revised to remove outside-use indications.

    Product
    VariaBreeze; Catalog number: 7300-0035-2. Podiatry: ablation, vaporization, incision, excision, and coagulation of soft tissue including matrixectomy, periungal and subungal warts, plantar warts, radical nail excision, and neuromas. The temporary increase of clear nail in
    Category
    Medical Device
    Distribution
    0 states