The Recall Desk

Hazard

Mis Labeling recalls

1,381 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

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.

126–150 of 1381

  • ModerateFDA (Drugs)·D-0095-2026·2025-10-29

    Cold remedy product label omits elderberry ingredient disclosure

    Church & Dwight is recalling Zicam Cold Remedy Medicated Fruit Drops because the label fails to disclose that bottles contain elderberry. The recall affects 21,912 bottles distributed nationwide.

    Product
    ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY — ZICAM COLD REMEDY MEDICATED FRUIT DROPS - ELDERBERRY (ZINC ACETATE ANHYDROUS, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0033-2026·2025-10-29

    Cetirizine Hydrochloride Tablets Recalled for Incorrect Imprint

    JB Chemicals and Pharmaceuticals Ltd is recalling Cetirizine Hydrochloride 10 mg tablets nationwide due to incorrect tablet imprinting. Affected lots: PY925014, PY925013, expiring 1/31/2028.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0228-2026·2025-10-29

    Synthes Retrograde Femoral Nailing Screw Recalled for Incorrect Packaging Length Labels

    Synthes (USA) is recalling 120 units of low-profile locking screws for femoral and tibial nailing systems due to incorrect external packaging labels. The 46mm screws are labeled as 42mm and vice versa, though the screws themselves are correctly marked.

    Product
    LOW PROF LCKNG SCREW, F/IM NAIL 5.0MM / L, 46MM / XL25/ STER. Product Code: 04.045.346TS. Used in RFN-ADVANCEDTM Retrograde Femoral Nailing (RFNA) System and the Tibial Nail Advanced System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0032-2026·2025-10-29

    Cetirizine Hydrochloride Tablets Recalled for Incorrect Tablet Imprinting

    Cetirizine Hydrochloride tablets distributed nationwide are being recalled due to incorrect imprinting. Consumers should stop using the product and contact their pharmacist or physician.

    Product
    CETIRIZINE HYDROCHLORIDE — CETIRIZINE HYDROCHLORIDE (CETIRIZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0226-2026·2025-10-29

    One Step Sterile Lancet Recalled Due to Missing or Incorrect UDI Codes

    Home Health US is recalling One Step Sterile Lancets due to missing or incorrect UDI codes on product labeling. Approximately 4,661 units were distributed nationwide through Amazon.

    Product
    One Step Sterile Lancet for Single Use (3 sizes): 06949517008861 30g 06949517008854 28g 06949517008847 23g The Lancing System is intended for the hygienic collection of capillary blood for testing purposes from the side of a fingertip and from alternative sites, such
    Category
    Medical Device
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-0023-2026·2025-10-22

    Hydromorphone injection recalled for incorrect or missing labeling information

    STAQ Pharma is recalling Hydromorphone HCL PF injections due to incorrect or missing lot numbers and expiration dates on product labels. Affected product was distributed nationwide.

    Product
    Hydromorphone HCL PF, 10mg/50 mL (0.2mg/mL) in NACL, Injection for IV use, 50 mL Syringe, STAQ Pharma Inc., 14135 E 42nd Ave, Denver, Colorado, NDC 73177-0104-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·26030·2025-10-16

    Wilteexs Bioethanol Fuel Bottles Recalled for Flash Fire Risk

    Wilteexs Bioethanol Fuel Bottles lack required flame mitigation devices, posing flash fire risk. About 1,100 units sold via Amazon April-July 2025; stop use immediately and contact Wilteexs for refund.

    Product
    Wilteexs Bioethanol Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0030-2026·2025-10-15

    Harris Teeter Cinnamon Texas Toast recall for undeclared milk allergen

    Harris Teeter has recalled Cinnamon Texas Toast due to undeclared milk in cheese and butter ingredients. The product lacks the required milk allergen statement, posing a risk to consumers with milk allergies.

    Product
    Harris Teeter CINNAMON TEXAS TOAST, NET WT 5.0oz (0.31g), INGREDIENTS BREAD*** CONTAINS WHEAT, UPC 0 72036 95734 4, Harris Teeter Raleigh, NC
    Category
    Food
    Distribution
    8 states
  • HighFDA (Food)·H-0013-2026·2025-10-15

    El Rojo Pasta De Harina Recalled for Missing Allergen Labeling

    El Rojo Pasta De Harina wheat pellets are recalled because the product lacks an ingredient list, failing to disclose wheat and Yellow No. 6. Consumers with allergies should not consume this product.

    Product
    El Rojo Pasta De Harina, Wheat Pellets. Net Wt 8 oz. (225g) UPC 0 35579-80871 6. Packaged and distributed by: El Rojo Wholesale, Maple Grove, MN 55469.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0071-2026·2025-10-15

    Toto S'Mores Cookie recalled for conflicting soy ingredient labeling

    Toto Foods recalls S'Mores Ooey Gooey Cookies due to conflicting label statements regarding soy content. The package contains contradictory information about whether the product includes or is free from soy.

    Product
    Toto S'Mores Ooey Gooey Cookie; Gluten Free & Dairy Free; Net Wt. 2.25 OZ Rear panel: Packed with superfoods; Gluten, Dairy & Soy Free UPC: 860010409398
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2592-2025·2025-10-08

    Medline Sterile Medical Device Convenience Kits Recalled for Missing Sterilization

    Medline Industries is recalling two sterile convenience kit models because the products were not sterilized despite being labeled as sterile. The kits were distributed to Florida, Maryland, New Jersey, and Tennessee.

    Product
    Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·H-0004-2026·2025-10-08

    Italian Sesame Cookies Recalled for Undeclared Allergen and Food Dyes

    Gina Marie Bakery LLC is recalling Italian Sesame Cookies due to undeclared sesame allergen and food dyes (Yellow 5, Red 40, Yellow 6). The recall affects 172 cases distributed in Connecticut.

    Product
    Italian Sesame Cookies
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0003-2026·2025-10-08

    Italian Mixed Vanilla Cookies Recalled for Undeclared Allergens and Colorings

    Gina Marie Bakery LLC is recalling Italian Mixed Vanilla Cookies (UPC 757808003169) due to undeclared almonds, sesame, and food colorings (Red 40, Red 3, Blue 1). Consumers with allergies to these ingredients should not consume the product.

    Product
    Italian Mixed Vanilla Cookies
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0001-2026·2025-10-08

    Orwashers Soho Sourdough Bread Recalled for Undeclared Sesame Seeds

    Orwashers brand Soho Sourdough XL Batard bread is being recalled because it may contain undeclared sesame seeds. This poses a risk to consumers with sesame allergies.

    Product
    Orwashers brand Soho Sourdough XL Batard; contains: wheat; 6-46.4oz PIECES PER CASE
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2640-2025·2025-10-08

    Hip Stem Implants Subject to Product Mix Recall

    Howmedica Osteonics has recalled EXETER V40 hip stem implants due to packaging errors where boxes may contain the wrong model or lot number. Affected units should be verified with surgical providers.

    Product
    1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0027-2026·2025-10-08

    Aesculap Elan 4 Duraguard Surgical Instruments Mislabeled Long and Standard

    Aesculap AG recalled three Elan 4 Fixed Duraguard surgical instruments that were mislabeled. Units marked 'Long' were actually 'Standard' and vice versa, which could affect surgical procedures.

    Product
    AESCULAP ELAN 4 FIXED DURAGUARD LONG. Model Number: GB943R.
    Category
    Medical Device
    Distribution
    0 states
  • ModerateFDA (Food)·H-0009-2026·2025-10-08

    Gina Marie Bakery Recalls Toasted Cherry Biscotti for Undeclared Red 40

    Gina Marie Bakery is recalling Toasted Cherry Biscotti because the product contains undeclared Red 40, a food coloring additive. Consumers with sensitivities to this ingredient should not consume the product.

    Product
    Toasted Cherry Biscotti
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·H-0008-2026·2025-10-08

    Vanilla Cookies Recalled for Undeclared Red 3 and Blue 1 Colorants

    Gina Marie Bakery LLC is recalling Vanilla Cookies with Raspberry Peach Jam due to undeclared Red 3 and Blue 1 food colorants. The recall affects 172 cases distributed in Connecticut.

    Product
    Vanilla Cookies with Raspberry Peach Jam
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-0026-2026·2025-10-08

    Aesculap Surgical Instrument Mislabeled Standard and Long Models

    The AESCULAP ELAN 4 FIXED DURAGUARD surgical instrument was mislabeled: Standard versions labeled as 'Long' and Long versions labeled as 'Standard.' The error affects units distributed to the US and multiple countries.

    Product
    AESCULAP ELAN 4 FIXED DURAGUARD STANDARD. Model Number: GB942R.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2618-2025·2025-10-01

    Extractor Pro RX Retrieval Balloon Catheter Recalled for Labeling Error

    Boston Scientific is recalling 156 units of Extractor Pro RX Retrieval Balloon Catheter due to a labeling error that incorrectly describes the skive hole position relative to the balloon.

    Product
    Extractor Pro RX Retrieval Balloon Catheter; UPN (REF): (1) M00547030 (9-12mm Below), (2) M00547000 (9-12mm Above);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2483-2025·2025-09-24

    3M Ranger Blood/Fluid Warming Sets recalled for clarification on operating parameters

    3M Company recalled 530,470 units of Ranger Blood/Fluid Warming High Flow Sets worldwide due to unclear documentation about flow rates and temperature parameters. The field action aims to clarify outlet temperature location and inlet fluid temperatures.

    Product
    3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355, 24370
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2590-2025·2025-09-24

    Foley Catheter Tray System Recalled Due to Incorrect Component Materials

    C.R. Bard is recalling 4,300 SureStep Foley Tray System units with incorrect catheter inserts that may mislead users about material type and antimicrobial coating, risking allergic reactions and infections.

    Product
    SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2589-2025·2025-09-24

    Foley Catheter Tray System Recalls Due to Incorrect Material Inserts

    SureStep Foley Tray System units contain incorrect inserts labeled incorrectly, risking patient allergic reactions and infections if the wrong material type is used.

    Product
    SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2591-2025·2025-09-24

    Foley Catheter Trays With Incorrect Material Identification Labels

    SureStep Foley catheter trays are being recalled because their inserts have incorrect material labels. Users may confuse latex with silicone or vice versa, which could cause allergic reactions or infections.

    Product
    SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
    Category
    Medical Device
    Distribution
    Distributed nationwide