The Recall Desk

Hazard

Mis Labeling recalls

9,622 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,622
Critical
163
Severe
590
Most recent
2026-09-24

Of the 9,622 mis labeling recalls we have scored against our rubric, 163 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 590 (6%) are Severe.

Which agencies issued them

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.

8876–8900 of 9622

  • HighFDA (Food)·F-1142-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond

    Food For Life Baking Company is recalling Ezekiel 4:9 Sprouted Grain Cereal because it may contain undeclared almonds, a major allergen.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Golden Flax, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL GOLDEN FLAX***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1191-2013·2013-03-20

    Bay Valley Foods Recalls Pasta Mix for Missing Soy Labeling

    Bay Valley Foods is voluntarily recalling approximately 430,227 cases of boxed pasta mix products because the labeling did not include soy lecithin in the ingredient statement.

    Product
    55613130643 Our Specialty Linguini & Parmesan, Linguini pasta with naturally flavored Parmesan & Romano Cheese Sauce Mix, Net WT 5.8 oz ( 164g), UPC 0 55049 00602 5, Distributed by S.T. Specialty Foods, Inc, Brooklyn Park, MN 55455.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1189-2013·2013-03-20

    Bay Valley Foods Recalls Pasta Mix for Missing Soy Labeling

    Bay Valley Foods is voluntarily recalling boxed pasta mix products because the ingredient labels failed to list soy lecithin.

    Product
    55613210946 Western Family, Easy Sides, Herb & Butter Pene, Net WT 5.5 oz (156 g), UPC "0 15400 12655 7", Proudly Distributed by Western Family Foods, Inc., P.O. Box 4057, Portland OR, 97208
    Category
    Food
    Distribution
    21 states
  • HighFDA (Food)·F-1141-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond

    Food For Life Baking Company is recalling Ezekiel 4:9 Sprouted Grain Cereal because it may contain undeclared almonds, a common allergen.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Original, 16 oz. Packaging label reads in part:"***Food FOR Life*** Ezekiel 4:9 SPROUTED WHOLE GRAIN CEREAL ORIGINAL NET WT. 16 OZ (454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434***".
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1061-2013·2013-03-20

    See's Candies Recalls Divinity Easter Eggs for Potential Peanut Mislabeling

    See's Candies is recalling 1.7 oz Divinity Easter Eggs with Walnuts because they may contain peanut butter instead of walnuts.

    Product
    See's Candies, Divinity with Walnuts; Net Wt. 1.7 oz, (48 gr). See's Candies, South San Francisco, CA.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·F-1143-2013·2013-03-20

    Food For Life Recalls Ezekiel 4:9 Cereal for Undeclared Almond Allergen

    Food For Life Baking Company is recalling specific lots of Ezekiel 4:9 Sprouted Grain Cereal because the product may contain undeclared almonds.

    Product
    Ezekiel 4:9 Sprouted Grain Cereal- Cinnamon Raisin, 16 oz. Packaging label reads in part:" Food FOR Life***EZEKIEL 4:9 SPROUTED WHOLE GRAIN CEREAL Cinnamon Raison***NET WT. 16 OZ(454g)***MANUFACTURED BY: FOOD FOR LIFE BAKING COMPANY, INC. P.O. BOX 1434 CORONA, CA 92878-1434**
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1190-2013·2013-03-20

    Bay Valley Recalls Angel Hair Pasta Mix for Missing Soy Labeling

    Bay Valley Foods is recalling Angel Hair Pasta with Herbs because the ingredient list failed to declare soy lecithin.

    Product
    556132100582 Meijer, Angel Hair Pasta with Herbs Angel Hair Pasta with Creamy Herb Sauce Mix , Net WT 4.8 oz ( 136g), UPC 7 19283 73636 95, Dist. by Meijer Distribution Inc., Grand Rapids, MI 49544.
    Category
    Food
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-0923-2013·2013-03-20

    Keystone Dental Recalls Mislabeled Genesis Straight Esthetic Abutments

    Keystone Dental Inc is recalling 35 units of Genesis Straight Esthetic abutments because they were mislabeled as 4.0 mm 1 mm cuff units when they are actually 5.0 mm 3 mm cuff units.

    Product
    Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: G71200 Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0927-2013·2013-03-20

    Innominata Lyme Disease Microplate EIA Kit Recalled for Low-Reactivity Issues

    Innominata dba GenBio is recalling 195 units of the Anti-Borrelia (Lyme) Microplate EIA Kit due to multiple incidents of low-reacting assay plates.

    Product
    ANTI-BORRELIA (LYME) MICROPLATE EIA Kit, Catalog # 32507 Kit Lot Number 120960. Package Insert Supplement: Calibrator-1206 U/mL, Positive Control-228 - 532 U/mL, and Negative Control-<120 U/mL; Manufactured by Innominata dba GenBio for Bio-Rad. The kit is used as an aid in diag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0929-2013·2013-03-20

    Abbott Recalls Mislabeled AMO Sensar Intraocular Lenses

    Abbott Medical Optics is recalling 155 AMO Sensar Intraocular Lenses because two production orders contained mislabeled units. The lenses are distributed worldwide.

    Product
    AMO Sensar Intraocular Lenses (IOLs), Model AR40e, Sensar Foldable IOL with OptiEdge Product Usage: These are ultraviolet-absorbing posterior chamber intraocular lenses for use after cataract extraction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0944-2013·2013-03-20

    Smith & Nephew Recalls Mislabelled Trigen Internal Hex Reconstruction Screws

    Smith & Nephew is recalling 90 units of Trigen internal hex reconstruction screws because 75 mm and 80 mm lengths were packaged in incorrect boxes and labels.

    Product
    INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162375, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 75 MM, TITANIUM, Smith & Nephew, Inc. Orthopedic. Bone screw for intramedullary rod fixation.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0924-2013·2013-03-20

    Keystone Dental Recalls Mislabeled Genesis Straight Esthetic Abutments

    Keystone Dental Inc is recalling 22 units of Genesis Straight Esthetic abutments that were mislabeled with incorrect dimensions.

    Product
    Genesis Straight Esthetic 5.0 mm 3. mm Cuff Abutment Part Number: G71205 Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1062-2013·2013-03-20

    LYFE Kitchen Sweet Corn Chowder Recalled for Incorrect Packaging Sleeve

    LYFE Kitchen is recalling Sweet Corn Chowder because some containers were packaged in sleeves labeled for Orange Carrot Ginger Soup. The product itself is correctly labeled.

    Product
    LYFE Kitchen, Sweet Corn Chowder with Cashew Cream, Yukon Gold Potatoes and Bell Peppers; 28 oz. 680 gr, Keep Refrigerated. UPC 855764003527 Del Monaco Specialty Products, Morgan Hill, CA
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0932-2013·2013-03-20

    Spine Smith Partners Recalls Cynch Lordotic T-PLIF Implants Due to Marking Error

    Spine Smith Partners LP is recalling three Cynch Lordotic T-PLIF implants distributed in Texas because they were incorrectly laser marked as 23mm instead of 28mm.

    Product
    Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
    Category
    Medical Device
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0938-2013·2013-03-20

    Synthes Spine Pedicle Screw Recalled for Incorrect Length Etching

    Synthes USA HQ, Inc. is recalling 18 units of 45 mm Click 'X Pedicle Screws because they were incorrectly etched as 40 mm.

    Product
    Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Core 40 mm Thread Length, Part Number 487.072. Intended to provide precise and segmental stabilization of the spine in skeletally mature patients.
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0943-2013·2013-03-20

    Smith & Nephew Recalls Mislabelled Trigen Internal Hex Reconstruction Screws

    Smith & Nephew is recalling 69 Trigen internal hex reconstruction screws because 75 mm and 80 mm units were packaged in incorrect boxes and labels.

    Product
    INTERNAL HEX RECON SCREW, TI-6AL-4V, REF 7162380, TRIGEN (R) INTERNAL HEX CAPTURED RECON SCREW, QTY: (1), 6.4 MM, 80 MM, TITANIUM, Smith & Nephew, Inc. Orthopedic. Bone screw for intramedullary rod fixation.
    Category
    Medical Device
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-192-2013·2013-03-20

    K C Pharmaceuticals Recalls Eye Drops With Incorrect Back Labeling

    K C Pharmaceuticals is recalling 31,704 bottles of Eye Drops advanced relief because the back labels fail to list three active ingredients.

    Product
    Eye Drops advanced relief (Dextran 70 0.1%, Polyethylene glycol 400 1%, Povidone 1%, Tetrahydrozoline HCl 0.05%) ophthalmic solution, 1/2 fl oz (15 mL) bottle, Distributed By Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0937-2013·2013-03-20

    Vygon Recalls 210 CT PICC Kits Packaged with Incorrect Needles

    Vygon Corporation is recalling 210 units of 6F Triple Lumen CT PICC kits because they were packaged with non-safety needles instead of the safety needles indicated on the label.

    Product
    Churchill Medical Systems, Inc. A Vygon Company - All sizes of CMS-CT6T225 6F Triple Lumen CT PICC with M.S.T. Components, Peripherally Inserted Central Catheter.
    Category
    Medical Device
    Distribution
    1 state
  • LowFDA (Devices)·Z-0933-2013·2013-03-20

    Siemens Total Iron Binding Capacity Reagent Cartridge Recall for Labeling Error

    Siemens is recalling Total Iron Binding Capacity reagent cartridges because the stated analytical sensitivity in the instructions is no longer valid.

    Product
    Siemens Total Iron Binding Capacity (IBCT) Flex Reagent Cartridge. An in vitro diagnostic test intended to quantitatively measure Total Iron Binding Capacity in human serum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-200-2013·2013-03-20

    Fresenius Kabi Recalls Calcium Glucosate Injection Due to Missing Label

    Fresenius Kabi USA LLC is recalling 155,900 vials of Calcium Glucosate Injection, USP, 10% due to missing labels. The recall is nationwide.

    Product
    CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive Use Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- Product Code 31110, NDC 63323-311-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1057-2013·2013-03-13

    R-Kane Z Pro High Protein Supplement Recalled for Undeclared Allergens

    R-Kane Products Inc. is recalling Z Pro 25 High Protein Supplement because the individual packets contain undeclared milk and soy allergens.

    Product
    Z Pro 25 High Protein Supplement Net. Wt. 1.5 oz. - Chocolate Flavor Formulated and Distributed by: R-Kane Products, Inc. 8351 National Highway, Pennsauken, NJ 08110
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1059-2013·2013-03-13

    Herbalife Formula 1 Vanilla Dream Shake Mix Recalled for Undeclared Milk

    Herbalife is recalling Formula 1 Vanilla Dream Shake Mix packets due to trace amounts of undeclared milk protein.

    Product
    HERBALIFE Formula 1 Instant Healthy Meal, Nutritional Shake Mix ( Vanilla Dream) Packets; net WT 1.83 oz/52 g; packaged as 12 packets in a cardboard carton; just add water; single serve powder in a packet;
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1055-2013·2013-03-13

    Bruce Foods Recalls Enchilada Sauce for Undeclared Soy and Wheat

    Bruce Foods Corp is recalling Food Club Mexican Style Enchilada Sauce due to undeclared soy and wheat allergens.

    Product
    Food Club(R) MEXICAN STYLE ENCHILADA SAUCE, RED, NET WT 10 OZ (284g), DISTRIBUTED BY TOPCO ASSOCIATES LLC, 7711 GROSS POINT RD., SKOKIE, IL 60077 UPC: 036800292208
    Category
    Food
    Distribution
    3 states