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.

151–175 of 1381

  • ModerateFDA (Food)·H-0620-2025·2025-09-24

    Goldband Snapper fillets recalled due to species misidentification

    E&E Foods is recalling Goldband Snapper fillets because testing confirmed the fish is actually Sharptooth Snapper, a different species. Consumers should return the product or discard it.

    Product
    Goldband Snapper Pristipomoides spp Fillets Skin-on Frozen, size 8-10oz, , item #991900011, individually Vacuum Package (IVP) portions in a plain white cardboard box, net wt. 10 lbs. per box. Product is wild caught, product of Indonesia, distributed by E&E Foods, Renton, WA.
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-2580-2025·2025-09-24

    Frontier Devices Distraction Pins Recalled for Unvalidated Shelf Life Labeling

    Folsom Metal Products is recalling Frontier Devices 14 mm Distraction Pins because the labeled shelf life has not been validated. The recall affects products distributed nationwide from August 2020 through July 2025.

    Product
    Frontier Devices, REF: 301.914S2, 14 mm Distraction Pin, 10 double packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2577-2025·2025-09-24

    Frontier Devices 12 mm Distraction Pins Recalled for Unvalidated Shelf Life Labeling

    Folsom Metal Products is recalling Frontier Devices 12 mm Distraction Pins due to labeling that includes unvalidated shelf life. The recall affects 160 units distributed nationwide from August 2020 through July 2025.

    Product
    Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0589-2025·2025-09-24

    Fish Oil Supplement Recalled for Unapproved Drug Claims

    Hi-Tech Pharmaceuticals fish oil supplement (85,950 units, Lot 517120551) is recalled for making unapproved drug claims on its label regarding cardiovascular health, joint pain, and cognitive function.

    Product
    HI-TECH PHARMACEUTICALS FISH OIL HEART AND BRAIN HEALTH EPA/DHA OMEGA 3 FATTY ACIDS SUPPORTS CARDIOVASCULAR HEALTH MAY HELP WITH JOINT PAIN MAY IMPROVE COGNITIVE FUNCTION 90 SOFT GELS UPC 8 11836 02585 9 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071
    Category
    Drug
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-2532-2025·2025-09-17

    Fortress Introducer Sheath System Recalled for Incorrect Pouch Label

    Fortress Introducer Sheath System units may have been packaged with pouch labels showing incorrect device size information, affecting 2,500 units distributed in the US and internationally.

    Product
    Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number: 386594 Product Description: Fortress Introducer Sheath System, 6F Straight 45cm:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0561-2025·2025-09-10

    Chocolate Mint Fudge Recalled for Missing Egg Allergen Labeling

    The Candy Barn is recalling Chocolate Mint Fudge packages because they do not list egg as an allergen in the ingredient statement, posing a risk to consumers with egg allergies. Affected products were distributed to stores in Kalona, Iowa.

    Product
    Chocolate Mint Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0559-2025·2025-09-10

    The Candy Barn Chocolate Fudge Recalled for Unlabeled Egg Allergen

    The Candy Barn is recalling chocolate fudge because egg is not listed on the label despite being present in the product. Consumers with egg allergies could face serious health risks.

    Product
    Chocolate Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·H-0568-2025·2025-09-10

    Lemon Meringue Pie Recalled for Undeclared Yellow#5 Food Dye

    Jessie Lord Bakery is recalling lemon meringue pie products sold across multiple states because they contain undeclared Yellow#5 (Tartrazine), a food coloring that may trigger allergic reactions in sensitive individuals.

    Product
    Lemon Meringue Pie, 8" round. Net Wt. 27 OZ; Refrigerate after opening Item Code 31811; UPC: 8 85523 31811 1;Jessie's Lemon Meringue Pie Sugar Free Item Code 30811; UPC: 8 85523 30811 2; Jessie's Lemon Meringue Pie Item Code 08276; UPC: 0 41512 08275 7; First street Lemon Mering
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·H-0560-2025·2025-09-10

    Chocolate Walnut Fudge recalled for undeclared walnut and egg allergens

    The Candy Barn recalls 665 packages of Chocolate Walnut Fudge due to missing allergen labeling. Products do not declare walnut and egg on the package label despite containing these allergens.

    Product
    Chocolate Walnut Fudge, The Candy Barn, 1113 Palm Ave Riverside, IA 52327, Net Wt: 4oz, 10oz, packed in plastic clamshell
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2517-2025·2025-09-10

    FloPatch FP120 Flowmeter Patch Recalled for Incorrect Expiry Date on Packaging

    Flosonics Medical is recalling the FloPatch FP120 flowmeter patch due to an incorrect expiry date printed on the outer shipping packaging. The package label reads 2025-06-20 instead of the correct 2026-06-20.

    Product
    FloPatch FP120, REF: FP120-FOT01-005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0531-2025·2025-09-03

    Breadman Bakery Multigrain Bread Recalled for Undisclosed Sesame Allergen

    Breadbox Co. is recalling Breadman Bakery Multigrain 24oz. loaves distributed in Los Angeles because the product label does not disclose sesame seed as an ingredient. Consumers with sesame allergies face potential allergic reactions.

    Product
    Breadman Bakery; Multigrain 24oz. Baked for Breaman-Melrose Bakery Inc. UPC# 8 6000947952 4
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-0599-2025·2025-09-03

    Lisdexamfetamine Dimesylate capsules recalled nationwide for dosage strength label error

    Lannett Company Inc. is recalling 8544 bottles of Lisdexamfetamine Dimesylate 40mg capsules distributed nationwide. Bottles labeled as 40mg capsules actually contain 30mg capsules.

    Product
    LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0525-2025·2025-09-03

    Gelson's Hummus Recall Due to Missing Refrigeration Storage Instructions

    Gelson's hummus products are being recalled due to missing refrigeration storage instructions on the label. Affected consumers should verify their lot codes and take appropriate precautions.

    Product
    Gelson's Hummus; Mediterranean Old World Family Recipe California-Made No Added Oils NET WT 8OZ (226g) UPC: 23631-10261
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Drugs)·D-0605-2025·2025-09-03

    Rite Aid Isopropyl Alcohol Prep Pads Recalled for Below-Labeled Concentration

    Rite Aid pharmacy isopropyl alcohol prep pads distributed nationwide are being recalled because the alcohol concentration falls below the labeled level. The FDA classified this Class II recall because reduced potency may affect the product's antimicrobial effectiveness.

    Product
    ALCOHOL — ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0524-2025·2025-09-03

    Gelson's Hummus Recalled for Missing Storage Instructions

    Gelson's Hummus products sold in Southern California are being recalled because product labels lack 'keep refrigerated' storage instructions. Consumers should discard recalled lots or ensure proper refrigeration has been maintained.

    Product
    Gelson's Hummus; Low Sodium No Cholesterol Classic NET WT 10OZ (283g) UPC: 23631-10260
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·H-0532-2025·2025-09-03

    Passionflower Herb Powdered Extract Recalled Due to Misbranding

    Martin Bauer, Inc. is recalling Passionflower Herb Powdered Extract 4% due to misbranding of the ingredient. The affected product was distributed to a consignee in North Carolina.

    Product
    Passionflower Herb Powdered Extract 4%, bulk packaging, individual large box, corrugated cardboard box with plastic liner .
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Devices)·Z-2402-2025·2025-09-03

    Philips Ultrasound L12-5 Transducer Probe Recall for Labeling Clarification

    Philips is recalling 171,322 L12-5 ultrasound transducer probes distributed nationwide to provide clarification and proper labeling defining the device's useful life.

    Product
    TRANSDUCER L12-5 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2360-2025·2025-09-03

    C9-2 Ultrasound Transducer Probe Useful Life Labeling Clarification

    Philips Ultrasound recalls 171,322 C9-2 Transducer Probe units to provide clarification and labeling defining the useful life of these medical ultrasound transducers. No illnesses or injuries have been reported.

    Product
    C9-2 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2405-2025·2025-09-03

    Philips Ultrasound VL13-5 Transducer Labeling Clarification

    Philips Ultrasound is clarifying labeling on 171,322 VL13-5 transducer probes distributed nationwide to better define the useful life of the equipment.

    Product
    VL13-5 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2381-2025·2025-09-03

    Philips L8-4 Transducer Probe labeling clarification on useful life

    Philips Ultrasound is recalling 171,322 L8-4 Transducer Probes to provide clarification and labeling defining the useful life of the ultrasound transducers.

    Product
    L8-4 Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2398-2025·2025-09-03

    Philips S8-3t Transducer Probe Labeling Clarification for Useful Life

    Philips Ultrasound is recalling approximately 171,322 S8-3t Transducer Probes distributed nationwide in the US to provide clarification and labeling regarding the device's useful life.

    Product
    S8-3t Transducer Probe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0511-2025·2025-08-27

    Blueberry Fritter Recalled Due to Undeclared Egg Allergen

    Hillside Orchard Farms is recalling Blueberry Fritters due to undeclared egg. The product was distributed to five states and poses a risk to consumers with egg allergies.

    Product
    Blueberry Fritter Net Wt 7 oz (198g) CONTAINS: MILK, SOY, WHEAT. Made By: Hillside Orchard Farms 105 Mitcham Circle Tiger, GA 30576
    Category
    Food
    Distribution
    5 states