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.

51–75 of 1381

  • ModerateFDA (Devices)·Z-1562-2026·2026-03-18

    Medline Chest Drainage Units: Instructions Clarified for Adult Use Only

    Medline is clarifying instructions for Aqua-Seal Chest Drainage Units to specify they are intended for adults 18 years and older. Approximately 2,894 units distributed worldwide are affected.

    Product
    Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model Number: DYNJ910851
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1502-2026·2026-03-18

    Penner Pacific Bathing Spa recalled for missing unique device identifier

    Penner Patient Care, Inc. is recalling 45 units of the Penner Pacific Bathing Spa (Model 360020-1P) distributed nationwide due to missing unique device identifiers (UDI).

    Product
    Penner Pacific Bathing Spa, Model Numbers 360020-1P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0545-2026·2026-03-18

    C2O Coconut Water with Pulp 15-pack with incorrect outer box labels

    The outer cardboard box of C2O Coconut Water with Pulp (17.5 oz) 15-packs contains incorrect Nutrition Facts and Ingredient Lists that fail to disclose 5g of added sugar per can, although the can itself has correct labeling.

    Product
    C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1492-2026·2026-03-11

    Vascular Prostheses Recalled Due to Incorrect Expiration Date Labeling

    Vascutek vascular prostheses (Gelsoft Plus and Gelweave) were mislabeled with incorrect expiration dates, with devices marked to expire one month later than they actually will. The labeling used packaging date instead of gel impregnation date for shelf-life calculation.

    Product
    Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, 631608PE, 631206PE, 631407P50E, 631508PE, 636008PE, 636006PE, 632518PE, 634008PE, 634006PE, 631218PE, 632211PE, 634007PE, 633006PE,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0574-2026·2026-03-11

    Karns Foods Mini Dark Chocolate Raspberry Cups recalled for undeclared peanuts

    Karns Prime And Fancy Foods is recalling Mini Dark Chocolate Raspberry Cups because they may contain undeclared peanuts. The product was distributed only in Pennsylvania.

    Product
    Karns Foods, Mini Dark Chocolate Raspberry Cups, 8 oz Clear plastic tamper evident packs, 36-42 packed per breakout
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-1487-2026·2026-03-11

    CS300 IABP battery runtime and cycle specifications require correction

    Datascope Corp. is updating battery runtime and cycle specifications in the CS300 IABP Instructions for Use. No illnesses or injuries reported.

    Product
    CS300 IABP. Software Version CS300 IABP C.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0523-2026·2026-03-04

    Tiki Bar Candy Recalled for Unlabeled Peanut Allergen Risk

    J2C Hawaii LLC recalls Tiki Bar Candy (Dark Chocolatey Peanut Butter & Pretzel) sold in Hawaii because the product label fails to declare peanuts in the required allergen statement despite containing peanut ingredients.

    Product
    Tiki Bar Candy Dark Chocolatey Peanut Butter & Pretzel. Net wt: Approx: 2 oz (57g). UPC 8 55725 00514 0. Taste of Maui Snacks dba of J2C Hawaii, LLC PO Box 1023, Wailuku HI 96793. The product label is read in parts: ***INGREDIENTS: Sugar***Whey Powder, Nonfat Milk Powder, Soy Le
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1459-2026·2026-03-04

    Knee and Humeral Socket Implants Recalled for Incorrect Labeling

    Encore Medical is recalling EMPOWR 3D KNEE implants due to incorrect labeling. Patients and healthcare providers should contact the manufacturer for guidance.

    Product
    Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 7L 16MM, VE Model/Catalog Number: 341-16-707
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1458-2026·2026-03-04

    Reverse Shoulder Prosthesis Implants Recalled for Incorrect Labeling

    Encore Medical is recalling RSP HUMERAL SOCKET INSERT implants (Model 509-00-432, Lot 385P1263) due to incorrect labeling. The implants were distributed nationwide across multiple states.

    Product
    Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP HUMERAL SOCKET INSERT, 32MM +4MM, STANDARD HXe-plus Model/Catalog Number: 509-00-432
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0526-2026·2026-03-04

    YO!MAN Lettuce Recalled Due to Undeclared Cyclamate

    Tengen USA Trading Corp is recalling 26 cases of YO!MAN Lettuce (Spicy Flavor) distributed in NY, PA, FL, LA, and TX because the product contains undeclared cyclamate, an ingredient not listed on the package.

    Product
    YO!MAN LETTUCE (SPICY FLAVOR); Ingredients: Lettuce, chili pepper, edible vegetable oil, salt, water, sugar, food additives (monosodium glutamate, potassium sorbate, streptoccoccus lactis, sodium dehydroacetate, sodium D-isoacsorbate, disodium ethylenediaminetetraacetatic acid,
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1460-2026·2026-03-04

    Knee and Shoulder Implants Recalled for Incorrect Labeling

    Encore Medical is recalling both knee and shoulder implants due to incorrect labeling. Affected patients should contact their healthcare provider for guidance.

    Product
    Brand Name: Reverse Shoulder Prosthesis (RSP) Product Name: RSP STANDARD HUMERAL SOCKET INSERT, 36MM, HXe-plus Model/Catalog Number: 509-00-036
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26284·2026-02-26

    Royal Oak Flame Saber lighters recalled for missing child-resistant mechanism

    Royal Oak Flame Saber lighters are missing required child-resistant safety mechanisms, violating mandatory standards. About 190,560 units were sold nationwide through major retailers from November 2023 to October 2025.

    Product
    Royal Oak Flame Saber Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0537-2026·2026-02-25

    Dietary Supplement Sleep Formula Recalled for Undeclared Milk Allergen

    Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset are being recalled for failing to declare milk allergen on the label, despite containing bovine colostrum. This poses a risk to milk-allergic consumers.

    Product
    Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-1426-2026·2026-02-25

    Prodisc C SK Cervical Implants Recalled for Mislabeling of Device Size

    Centinel Spine is recalling 20 Prodisc C SK cervical disc replacements because units were mislabeled as 6mm but contained 5mm products. Affected devices were distributed in multiple US states.

    Product
    Brand Name: Prodisc Product Name: Prodisc C SK Model/Catalog Number: PDSL6 Software Version: N/A Product Description: Total cervical disc replacement Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26273·2026-02-19

    Joly's 80% Vinegar Recalled for Missing Safety Labels and Hazards

    Joly's 80% Vinegar lacks required safety labels and first-aid instructions, posing risks of poisoning and chemical burns. Approximately 450 bottles sold on Amazon from May to November 2025 are affected.

    Product
    Joly's 80% Vinegar (32 oz, pack of two)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0506-2026·2026-02-18

    Karison brand Punjabi Pinni recalled for undeclared milk allergen

    Karison brand Punjabi Pinni (12 oz) is recalled because milk, a common allergen, is not listed on the ingredient label. The product was distributed in NY, NJ, and VA.

    Product
    Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that p
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1357-2026·2026-02-18

    Newborn Heart Rate Monitor Cap Has Incorrect Sizing Labeling

    Surepulse Medical recalls VS Cap Small components of newborn heart rate monitors due to incorrect sizing guidance in the labeling. The labeling error could affect proper device fit.

    Product
    Surepulse VS Cap Small REF: SP-160-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1359-2026·2026-02-18

    Surepulse VS Cap Large Medical Device Recalled for Incorrect Sizing Guide

    Surepulse Medical is recalling the VS Cap Large, a component of the VS Newborn Heart Rate Monitor, due to incorrect sizing information in the labeling.

    Product
    Surepulse VS Cap Large REF: SP-162-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1360-2026·2026-02-18

    Surepulse VS Cap Extra Large Recalled for Incorrect Sizing Guide

    The Surepulse VS Cap Extra Large component of newborn heart rate monitors has been recalled because the product labeling contains an incorrect sizing guide.

    Product
    Surepulse VS Cap Extra Large REF: SP-163-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0306-2026·2026-02-18

    Tablets of Doxazosin Mesylate 4 mg Recalled for Incorrect Imprinting

    Unichem Pharmaceuticals is recalling 60,000 Doxazosin Mesylate 4 mg tablets due to incorrect imprinting. Patients should check their medication bottles and contact their pharmacy if they have Lot #GDSH25006.

    Product
    DOXAZOSIN MESYLATE — DOXAZOSIN MESYLATE (DOXAZOSIN MESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1358-2026·2026-02-18

    FDA Recalls Surepulse Newborn Heart Rate Monitor Cap for Labeling Error

    Surepulse Medical is recalling certain newborn heart rate monitor caps due to incorrect sizing information in the labeling. The issue affects specific lot numbers distributed in the US and internationally.

    Product
    Surepulse VS Cap Medium REF: SP-161-A1 component of VS Newborn Heart Rate Monitor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0500-2026·2026-02-11

    Bread and Roll Mix Recalled for Undeclared Milk Allergen

    B.C. Williams Bakery Service is recalling Bread and Roll Mix sold nationwide due to undeclared milk allergen. Consumers with milk allergies could have serious allergic reactions if they consume this product.

    Product
    Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1237-2026·2026-02-11

    Surgical screws recalled due to labeling error and size mismatch

    A lot of Tornier surgical screws is labeled as 5.0mm x 18mm but actually measures 5.0mm x 14mm. If undetected during surgery, the incorrect screw could increase the risk of mechanical failure and require revision surgery.

    Product
    TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX18MM NON STERILE, catalog number DWJ318
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0446-2026·2026-02-11

    Ketchup recall: undeclared quinine ingredient poses health risk

    Prima Foods is recalling BarbaCuban Ram Air Red Zesty Ketchup due to undeclared quinine. The product was distributed in Florida; consumers should not consume and should dispose of the product.

    Product
    BarbaCuban Ram Air Red Zesty Ketchup, Net Wt. 12 oz (355 ml) 12 oz glass bottles, and 1 gallon HDPE Industrial Plastic Jugs, ¿ gallon HDPE Industrial Plastic Jugs. packaged in 12x12 fl oz, 6x12 fl oz, 4x1 gallon, 4x1/2 gallons. UPC code 0 07196 60000 7
    Category
    Food
    Distribution
    0 states