The Recall Desk

Hazard

Mis Labeling recalls

9,611 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,611
Critical
161
Severe
589
Most recent
2026-09-24

Of the 9,611 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 589 (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.

7401–7425 of 9611

  • HighFDA (Food)·F-1900-2014·2014-05-07

    Pastene Italian Rigatoni Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene Italian Rigatoni #31 because the semolina pasta fails to declare the allergen wheat.

    Product
    Pastene ITALIAN RIGATONI #31 , 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7083 UPC: 066086070832
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1905-2014·2014-05-07

    Pastene Semolina Pasta Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene ITAL NIDI #81 pasta because the product fails to declare the wheat allergen.

    Product
    Pastene ITAL NIDI #81 ,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7090 UPC: 066086070900
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1902-2014·2014-05-07

    Pastene Italian Ditali Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling 6,000 cases of Pastene Italian Ditali #45 pasta because the product fails to declare the allergen wheat.

    Product
    Pastene ITALIAN DITALI #45 , 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7085 UPC: 066086070856
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1893-2014·2014-05-07

    Pastene Tagliatelle Verdi Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling 6,000 cases of Pastene ITAL Tagliatelle Verdi #80 because the semolina pasta fails to declare the allergen wheat.

    Product
    Pastene ITAL TAGLIATELLE VERDI #80, 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7070 UPC: 066086070702
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1889-2014·2014-05-07

    Pastene Mafaldine Pasta Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene Mafaldine pasta because the product fails to declare the allergen wheat.

    Product
    Pastene MAFALDINE 5, 16 oz cellophane bag Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number: 7062 UPC: 066086070627
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1892-2014·2014-05-07

    Pastene Farfalline Pasta Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling 16 oz bags of Farfalline pasta because the product fails to declare the allergen wheat.

    Product
    Pastene FARFALLINE 78, 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number: 7067 UPC: 066086070672
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1903-2014·2014-05-07

    Pastene Italian Stelline Pasta Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling 16 oz bags of Italian Stelline pasta because the product fails to declare the allergen wheat.

    Product
    Pastene ITALIAN STELLINE #59 , 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7086 UPC: 066086070863
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1896-2014·2014-05-07

    Pastene Italian Linguine Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling 16 oz bags of Italian Linguine #6 because the product fails to declare the allergen wheat.

    Product
    Pastene ITALIAN LINGUINE #6, 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7077 UPC: 066086070771
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1907-2014·2014-05-07

    Pastene Italian Pappardelle Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene Italian Pappardelle because the semolina pasta fails to declare the allergen wheat.

    Product
    Pastene ITALIAN PAPPARDELLE ,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7092 UPC: 066086070924
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1899-2014·2014-05-07

    Pastene Italian Capellini Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene Italian Capellini #17 because the semolina pasta fails to declare the wheat allergen.

    Product
    Pastene ITALIAN CAPELLINI #17, 16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7082 UPC: 066086070825
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1912-2014·2014-05-07

    Pastene Semolina Pasta Recalled for Undeclared Wheat Allergen

    The Pastene Companies Ltd. is recalling Pastene ITAL SPIRAL TRI COLOR pasta because it fails to declare the allergen wheat.

    Product
    Pastene ITAL SPIRAL TRI COLOR,16 oz cellophane bag. Imported from Italy. Imported by the Pastene Company, Canton, MA Item Number:7093 UPC: 066086070931
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1526-2014·2014-05-07

    Medtronic External Neurostimulators Recalled for Cycling Feature Labeling Issue

    Medtronic is recalling external neurostimulators because current labeling indicates the cycling feature improves device longevity and recharge interval.

    Product
    Medtronic, External neurostimulator, ENS (37021) & ENS (37022). Including the external neurostimulators which are associated with software application run on the NVision Clinician Programmer and used during trialing for spinal cord stimulation (SCS) patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1518-2014·2014-05-07

    Siemens Recalls IMMULITE 2000 Total IgE Assays Due to Positive Bias

    Siemens Healthcare Diagnostics is recalling specific lots of IMMULITE 2000 Total IgE assays because they show a 23% positive bias against the WHO standard.

    Product
    IMMULITE 2000 /IMMULITE 2000 XPi Systems TIE Total IgE, REF L2KIE2, SMN 10380873, and L2KIE6, SMN 10380872, IVD --- Siemens Healthcare Diagnostics Products Ltd. For in vitro diagnostic use with the IMMULITE, IMMULITE 1000, and IMMULITE 2000/ IMMULITE 2000 XPi Systems Analyzers
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·F-1914-2014·2014-05-07

    Rising Moon Organics Pesto Ravioli Recalled for Missing Pine Nut Allergen Labeling

    Carmel Food Group is recalling Rising Moon Organics Basil, Asiago & Pine Nut Pesto Ravioli because the packaging incorrectly omits pine nuts from the allergen statement.

    Product
    RISING MOON ORGANICS BASIL ASIAGO PINE NUT PESTO RAVIOLI; 8 OZ PACKAGE (227g) Keep Frozen USDA Organic: Distributed by Rising Moon Organics 313 Iron Horse Way Providence, RI 02908
    Category
    Food
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-1525-2014·2014-05-07

    Medtronic Activa Neurostimulators Recalled for Cycling Feature Labeling

    Medtronic is recalling Activa neurostimulators because current labeling indicates the cycling feature improves device longevity and recharge interval.

    Product
    Medtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Activa PC+S (37604), Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation for movement disorders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1532-2014·2014-05-07

    Siemens Androstenedione Assay Recall Due to Over-Recovery

    Siemens recalls Androstenedione assays because they over-recover samples above 5.5 ng/mL, contradicting the stated 10 ng/mL limit.

    Product
    IMMULITE 2000/2000 XPi Systems Androstenedione (Test Code AND), REF L2KAO2, SMN 10381188, IVD, 200 test kit size --- Siemens Healthcare Diagnostics Products Ltd. Llanberis, Gwynedd, LL55 4EL, UK For in vitro diagnostic use with the IMMULITE/IMMULITE 1000 and 2000 Systems Ana
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1524-2014·2014-05-07

    Medtronic Neurostimulators Recalled for Cycling Feature Labeling Concerns

    Medtronic is recalling specific neurostimulators because current labeling indicates the cycling feature improves device longevity, a claim that may be inaccurate.

    Product
    Medtronic neurostimulators. Restore (37711), RestoreADVANCED (37713), RestoreADVANCED SureScan MRI (97713), RestoreSENSOR (37714), RestoreSENSOR SureScan MRI (97714), PrimeAdvanced SureScan MRI, (97702), RestoreULTRA (37712), RestoreULTRA SureScan MRI (97712), Itrel 4 (37703), It
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1531-2014·2014-05-07

    Siemens IMMULITE Androstenedione Assay Recalled for Over-Recovery

    Siemens recalls IMMULITE Androstenedione assays because they over-recover samples above 5.5 ng/mL, contradicting the stated 10 ng/mL linearity limit.

    Product
    IMMULITE/IMMULITE 1000 Systems Androstenedione (Test Code AND), REF LKAO1, SMN 10381158, IVD, 100 test kit size --- Siemens Healthcare Diagnostics Products Ltd. Llanberis, Gwynedd, LL55 4EL, UK For in vitro diagnostic use with the IMMULITE/IMMULITE 1000 and 2000 Systems Analy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1913-2014·2014-05-07

    Fish Oil Softgels Recalled Due to Mixed Conjugated Linoleic Acid Capsules

    Nutri-Force Nutrition is recalling Fish Oil Softgel Capsules because Conjugated Linoleic Acid capsules were found mixed in the bottles.

    Product
    Fish Oil Softgel Capsules in white High Density Poly-Ethylene bottles labeled in part: "Major [brand] Fish Oil Cholesterol Free 1000 MG *** 100 Softgels *** Distributed by Major Pharmaceuticals ***Livonia, MI 48150 USA ***".
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-1257-2014·2014-05-07

    John W Hollis Inc Recalls Phosphatidylcholine Injection Due to Labeling Error

    John W Hollis Inc is recalling 7 vials of Phosphatidylcholine Solution for Injection because the expiration date on the label is earlier than the date listed on the vial.

    Product
    Phosphatidylcholine Solution for Injection, 50 mg/ mL, 50 mL Vial, Rx Only, Not for Resale. John Hollis Pharmacy, 110 20th Avenue N, Nashville, TN 37203.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1536-2014·2014-05-07

    BD Biosciences Recalls Mislabeled Anti EpCAM PE Reagent Lots

    BD Biosciences is recalling two lots of Anti EpCAM PE reagent because the vials contain CD9 PE antibody instead of the labeled EpCAM antibody.

    Product
    Anti EpCam PE - Analyte Specific Reagent. Anti-EpCAM is directed against human epithelial adhesion molecule that has been identified as a 40 -kilodalton (kd) protein in Western Blotting.
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-1259-2014·2014-05-07

    John W Hollis Recalls Polidocanol 1% Solution Due to Incorrect Expiration Date

    John W Hollis Inc is recalling 2 vials of Polidocanol 1% Solution because the expiration date on the vial is earlier than the date listed on the label.

    Product
    Polidocanol 1% Solution, 50 mL Vial, Rx Only, Not for Resale. John Hollis Pharmacy, 110 20th Avenue N, Nashville, TN 37203.
    Category
    Drug
    Distribution
    4 states
  • LowFDA (Drugs)·D-1258-2014·2014-05-07

    John W Hollis Recalls Papaverine, Phentolamine, and Atropine Solution Vials

    John W Hollis Inc is recalling specific vials of Papaverine, Phentolamine, and Atropine solution due to an incorrect expiration date on the label.

    Product
    Papaverine 60 mg, Phentolamine 4 mg, and Atropine 0.3 mg Solution, 10 mL Vial, Rx Only. Not for Resale. John Hollis Pharmacy, 110 20th Avenue N, Nashville, TN 37203.
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Food)·F-1875-2014·2014-04-30

    CJ Bakery Recalls Cinnamon Manjoo Cookies for Undeclared Wheat

    CJ Bakery is recalling Cinnamon Cookie Manjoo products because they contain undeclared wheat, a major food allergen.

    Product
    Cinnamon Cookie Manjoo, 200g Net Weight. Packaged in clear plastic bag, 10 per bag. Product package labeled in part:"***Cinnamon Cookie (Manjoo)*** Net Wt. 200g, 7.1oz***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA 90040***22290392
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1489-2014·2014-04-30

    Ev3 Recalls EverCross PTA Dilatation Catheters Due to Labeling Error

    Ev3 is recalling two lots of EverCross PTA Dilatation Catheters because of a discrepancy in the balloon and delivery catheter lengths printed on the product labeling.

    Product
    ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 120mm x 135cm, REF: AB35W06120135. and ev3 EverCross 0.035" OTW PTA Dilatation Catheter, 6mm x 40mm x, 80cm REF: AB35W06040080. Peripheral Dilatation Catheter
    Category
    Medical Device
    Distribution
    6 states