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.

3876–3900 of 9607

  • ModerateFDA (Food)·F-0829-2018·2018-02-28

    Bob's Red Mill Organic Creamy Wheat Hot Cereal Recalled for Undeclared Wheat

    Bob's Red Mill is recalling Organic Creamy Wheat Hot Cereal because the back label incorrectly identifies the product as muffins, failing to declare wheat.

    Product
    Organic Creamy Wheat Hot Cereal, Item number 6097C244, Pack size: 24 oz bag, 4 bags in a case. UPC: 3997800992
    Category
    Food
    Distribution
    5 states
  • LowFDA (Devices)·Z-0664-2018·2018-02-28

    LivaNova Recalls Sorin Group Smart Perfusion Packs Due to Incorrect Expiration Date

    LivaNova USA is recalling 16 units of Sorin Group Smart Perfusion Pack E-Packs because they are labeled with incorrect expiration dates.

    Product
    Sorin Group Smart Perfusion Pack E-Pack, REF 088511400, Rev: L, Single Use, Sterile, Rx. The firm name on the label is Sorin Group USA, Inc., Arvada, CO.
    Category
    Medical Device
    Distribution
    1 state
  • CriticalFDA (Drugs)·D-0342-2018·2018-02-21

    Senna Laxative Tablets Recalled for Containing Naproxen Sodium

    Magno Humphries Laboratories is recalling Senna Laxative tablets that were mislabeled and contained Naproxen Sodium instead.

    Product
    Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0626-2018·2018-02-21

    Zimmer Biomet Recalls G7 Dual Mobility Hip Liners Due to Labeling Error

    Zimmer Biomet is recalling 8 units of G7 Dual Mobility Liners because they are labeled as 44mm but may physically be 42mm liners.

    Product
    G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0798-2018·2018-02-21

    Weis Markets Recalls Dried Beef Party Rye Dip for Undeclared Allergens

    Weis Markets is recalling Dried Beef Party Rye Dip because the label fails to list egg and milk, which are present in the ingredients.

    Product
    Weis Weis Markets, Inc., Sunbury, PA 17801-0471; Keep Refrigerated; Dried Beef Party Rye Dip; Ingredients: Hellman's Mayonaise, Sour Cream, Dried Beef (Cured with Water, Salt, Sugar, Sodium Nitrate, Sodium Nitrite), Parsley, Onion, Dill Weed; SELL BY RANGE up to 02/16/2018.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0591-2018·2018-02-21

    Aesculap Vega Knee Trial Plateau Recalled for Incorrect Labeling

    Aesculap is recalling 13 units of the NS357R Vega PS Tibia Trial/Preparation Plateau size T4 due to incorrect labeling. Using the wrong size could lead to implantation errors, ligament injury, pain, or revision surgery.

    Product
    NS357R Vega PS Tibia Trial/Preparation Plateau size T4 (Component of the Vega Knee System Set #ST0468) The affected part is provided in the Vega Knee System Set #ST0468. The Vega Knee System is used for reconstruction of the diseased knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0797-2018·2018-02-21

    General Mills Recalls Larabar Chocolate Chip Cookie Dough Bars

    General Mills is recalling Larabar Chocolate Chip Cookie Dough bars because they may contain individually wrapped Coconut Cream Pie Bars.

    Product
    Larabar Chocolate Chip Cookie Dough, 5 - 1.6 oz (45g) bars Net Wt 8.0 oz(226g), UPC 21908-48817. Case UPC 000-21908-41675-5
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0396-2018·2018-02-21

    Sage Products Recalls Q.CARE Oral Cleansing System Due to Cross-Contamination

    Sage Products Inc is recalling Q.CARE Oral Cleansing & Suctioning Systems because oral care solutions were manufactured on equipment shared with non-pharmaceutical products.

    Product
    Q.CARE Oral Cleansing & Suctioning System q4. Contains 1 Covered Yankauer, Suction Handle and Y-Connector, 2 Toothbrush packages with Antiplaque solution. 4 Suction Oral Swab packages with Perox-A-Mint solution. 2 Oropharyngeal Suction Catheter packages, Sage Products, Inc., 39
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0822-2018·2018-02-21

    Walnut Creek Foods Caramel Popcorn Recalled for Missing Soy Labeling

    Walnut Creek Foods is recalling Caramel Popcorn because the label failed to list soy lecithin as an ingredient.

    Product
    WALNUT CREEK FOODS Caramel Popcorn NET WT 15 OZ (425g) Ingredients: Evaporated Can Juice, Popcorn, Butter (cream, salt), Salt, Sodium Bicarbonate, Cream of Tartar Contains: Milk Distributed by: Walnut Creek Foods, Walnut Creek, OH 44687 UPC 25555 99857 2
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0612-2018·2018-02-21

    Zimmer Surgical Recalls A.T.S. 4000TS Tourniquet Systems for Labeling Updates

    Zimmer Surgical Inc is recalling 8,231 A.T.S. 4000TS Tourniquet Systems to update on-device labels and operator manuals, and to reduce the required separation distance from RF communication equipment.

    Product
    A.T.S. 4000TS Tourniquet Systems, Personalized Pressure. Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities. .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0613-2018·2018-02-21

    Zimmer Surgical Recalls A.T.S. 2200TS Tourniquet Systems for Labeling Updates

    Zimmer Surgical is recalling 8,231 A.T.S. 2200TS Tourniquet Systems to update on-device labels and operator manuals regarding RF communication equipment separation distances.

    Product
    A.T.S. 2200TS Tourniquet Systems, Personalized Pressure. Zimmer Surgical, Inc. Dover, OH 44622 Intended to be used by qualified professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0600-2018·2018-02-21

    ConforMIS Recalls Mislabeled Total Knee Replacement Implant Kits

    ConforMIS, Inc. is recalling two total knee replacement kits due to mislabeling. The affected units were distributed in California and Texas.

    Product
    Total Knee Replacement , Catalog/Model # TPS-111-1111, UDI: +M572TPS1111111021/$$+31712310398482- and +M572TPS1111111021/$$+31712310399917/ Intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0597-2018·2018-02-21

    OrthoPediatrics Recalls 7.0mm Pedicle Screws Due to Color Anodizing Error

    OrthoPediatrics Corp is recalling 24 units of 7.0mm x 40mm pedicle screws because they were color anodized with the same color used for 5mm screws.

    Product
    Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Usage: Posterior non-cervical pedicle screw fixation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0413-2018·2018-02-21

    Allergan Recalls NORCO Tablets Due to Missing Controlled Substance Labeling

    Allergan is recalling 8 bottles of NORCO tablets because the primary label is missing the required CII controlled drug classification indication.

    Product
    NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets, USP, 10 mg/325 mg, 100-count bottles, Rx Only, Distributed by: Allergan USA, Inc., Irvine, CA 92612, NDC 0023-6022-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0416-2018·2018-02-21

    Genentech Recalls Klonopin Tablets Due to Missing Schedule IV Labeling

    Genentech is recalling Klonopin (clonazepam) 0.5 mg tablets because the Schedule IV controlled substance indicator was omitted from the product carton.

    Product
    Klonopin (clonazepam) 0.5 mg Tablets,100-count bottle, Rx only. Made in Canada, Distributed by Genentech USA, Inc. A Member of the Roach Group, 1 DNA Way South San Francisco, CA 94080-4990. NDC 0004-0068-01
    Category
    Drug
    Distribution
    0 states
  • HighNHTSA·18V113000·2018-02-15

    Mercedes-Benz Recalls Sprinter Vans Due to Incorrect Weight Labels

    Daimler Vans USA is recalling 2016-2017 Mercedes-Benz Sprinter 2500 and 3500 vans with folding seats because the unloaded vehicle weight label may be incorrect, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0774-2018·2018-02-14

    Bulletproof Collagen Protein Recalled for Undeclared Milk Allergen

    Bulletproof 360 Inc is recalling Unflavored Collagen Protein because the product contains undeclared milk. The item is mislabeled as collagen protein but actually contains whey protein.

    Product
    Bulletproof Unflavored Collagen Protein High Performance Building Blocks Dietary Supplement, packaged in a 16-oz. composite-film bag, UPC: 8 15709 02115 3. The label is read in parts: "***COLLAGEN PROTEIN***Ingredients: Hydrolyzed collagen powder***Processed in a facility that
    Category
    Food
    Distribution
    14 states
  • SevereFDA (Drugs)·D-0333-2018·2018-02-14

    Flawless Beauty LLC Recalls Ling Zhi Capsules for Misbranding

    Flawless Beauty LLC is voluntarily recalling all lots of Ling Zhi capsules because they were marketed without an approved NDA/ANDA, constituting misbranding and unapproved new drugs.

    Product
    Ling Zhi capsules
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·010-2018·2018-02-14

    Saker ShopRites Recalls Pork and Chicken Empanadas Due to Undeclared Egg Allergen

    Saker ShopRites is recalling pork and chicken empanadas because they contain egg, a known allergen, which is not listed on the label. No injuries have been reported.

    Product
    Saker Shoprites Inc — Saker ShopRites, Inc. Recalls Empanadas due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0782-2018·2018-02-14

    Stevens Bakery Peach Pies Recalled for Undeclared Milk Allergen

    Stevens Family Bakery & Orchard LLC is recalling 15 baked peach pies sold in Ohio because the label failed to list butter, an undeclared milk allergen.

    Product
    Peach Pie Baked whole pies & Baked 1/2 pies, Stevens Bakery & Orchard, 7344 Thackery Road, Springfield, Ohio 45502, (937) 788-2873
    Category
    Food
    Distribution
    1 state