The Recall Desk

Hazard

Mis Labeling recalls

9,607 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
9,607
Critical
160
Severe
588
Most recent
2026-09-10

Of the 9,607 mis labeling recalls we have scored against our rubric, 160 (2%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 588 (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.

4651–4675 of 9607

  • ModerateFDA (Food)·F-2159-2017·2017-05-10

    Frozen Shrimp Recalled for Failure to Declare Sulfites

    Global Marketing Enterprises is recalling 1,173.19 lbs of frozen farm-raised head-on shrimps because the label does not declare the presence of sulfites.

    Product
    40/50 ct/kg (21/25 ct/lb) Farm Raised Head-On Shrimps, Keep Frozen, Must be fully cooked before serving. 1.02 kg, 2.24 lb. Packed by: Global Marketing Ent Inc, Chicago, IL 60616
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1937-2017·2017-05-10

    Anspach Effort Recalls Autolube-III Pneumatic Systems for Missing Service Interval

    The Anspach Effort, Inc. is recalling 17 Autolube-III pneumatic systems because the supplied directions for use did not include a recommended service interval.

    Product
    Autolube-III with Foot Guard Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1922-2017·2017-05-10

    Boston Scientific Recalls Mislabeled JETSTREAM Atherectomy Catheters

    Boston Scientific is voluntarily removing three lots of JETSTREAM atherectomy catheters because some units were mislabeled with incorrect sizes.

    Product
    The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease in the peripheral vasculature. The System includes multiple distal ports located at the catheter tip, which are designed to provide independent infusion and aspi
    Category
    Medical Device
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-1920-2017·2017-05-10

    Smith & Nephew Recalls Renovation Osteotome Blades Due to Shelf Life Data

    Smith & Nephew is recalling Renovation osteotome blades because stability data does not support the labeled 10-year shelf life.

    Product
    RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 20 MM, REF 71369420, STERILE R, QTY: (1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1958-2017·2017-05-10

    Anspach Effort 7.2cm Adjustable Drill Guide Recalled for Missing Service Interval

    The Anspach Effort, Inc. is recalling 198 units of the 7.2cm Adjustable Drill Guide because the supplied directions for use did not contain a recommended service interval.

    Product
    7.2cm Adjustable Drill Guide Product Usage: Electric system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2162-2017·2017-05-10

    Goya Octopus in Olive Oil Recalled for Squid Mislabeling

    Tradewind Foods is recalling Goya Octopus in Olive Oil because the product contains squid instead of octopus. This labeling error affects consumers in Puerto Rico and the Caribbean.

    Product
    Goya Octopus in Olive Oil, Pulpo en Aceite de Oliva, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 07096.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-2032-2017·2017-05-10

    Anspach Effort Recalls Heavy Duty Long Heavy Short Attachment

    The Anspach Effort, Inc. is recalling 206 units of the 20.2cm Heavy Duty Long Heavy Short Attachment because the supplied directions for use did not contain a recommended service interval.

    Product
    20.2cm Heavy Duty Long Heavy Short Attachment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1944-2017·2017-05-10

    Anspach Effort Recalls XMAX Pneumatic Drill System for Missing Service Interval

    The Anspach Effort, Inc. is recalling 554 XMAX Pneumatic Drill Systems because the supplied directions for use did not include a recommended service interval.

    Product
    XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2164-2017·2017-05-10

    Goya Octopus in Pickled Sauce Recalled for Squid Mislabeling

    Tradewind Foods is recalling Goya Octopus in Pickled Sauce because the product contains squid instead of octopus, as labeled.

    Product
    Goya Octopus in Pickled Sauce, Pulpo a la Marinera, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 07096.
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-2178-2017·2017-05-10

    Source Naturals Vitamin D-3 Recalled for Lower Concentrations

    Threshold Enterprises Ltd is recalling specific lots of Source Naturals Vitamin D-3 dietary supplements because testing found lower concentrations than labeled.

    Product
    Source Naturals Dietary Supplement Vitamin D-3; Bioactive Form for Bone and Immune Health 2000 IU per serving, 500% DV. Other ingredients: Vegetable Glycerin, Deionized water, citric acid, Natural orange flavor and lemon essential oil. Use 5 drops once daily in a drink. Pa
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1964-2017·2017-05-10

    Anspach Effort Recalls Adjustable Drill Guide for Missing Service Interval

    The Anspach Effort, Inc. is recalling six units of the Adjustable Drill Guide, Black Max because the supplied directions for use did not contain a recommended service interval.

    Product
    ADJUSTABLE DRILL GUIDE, BLACK MAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1895-2017·2017-05-10

    Richard-Allan Scientific Recalls Shandon Rapid Chrome Kwik-Diff Kits

    Richard-Allan Scientific is recalling Shandon Rapid Chrome Kwik-Diff Kits because the Methylene Blue Solution #3 was mislabeled and actually contained Crystal Violet.

    Product
    Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707 Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990700 is sold as a kit in 500ml bottles. Shandon Rapid Chrome Kwik-Diff Kit, Part Number 9990707 is sold as a
    Category
    Medical Device
    Distribution
    24 states
  • LowFDA (Drugs)·D-0695-2017·2017-05-10

    Fagron Recalls Zinc Oxide Paste Due to Labeling Error

    Fagron, Inc. is recalling Zinc Oxide Paste 25% because of an incorrect strength value in the Drug Facts Panel.

    Product
    Zinc Oxide Paste 25%, 500 g, For Prescription Compounding, Fagron Inc.2400 Pilot Knob Rd, St. Paul, MN 55120m NDC 51522-0694-5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·046-2017·2017-05-08

    Ford Brothers Recalls Beef Patties for Undeclared Soy Allergen

    Ford Brothers Wholesale Meats is recalling beef patties because they contain soy, a known allergen, that is not declared on the label.

    Product
    Ford Brothers Wholesale Meats Inc — Ford Brothers Wholesale Meats, Inc. Recalls Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • ModerateNHTSA·17V304000·2017-05-04

    Hino 338 Trucks Recalled for Incorrect Certification Labels

    Jim Reed's Truck Sales is recalling 2014-2016 Hino 338 trucks because certification labels fail to identify the final stage manufacturer, potentially hindering safety recall awareness.

    Product
    HINO — HINO 338
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-2116-2017·2017-05-03

    Valley Bakery Hamburger Buns Recalled for Undeclared Egg Allergen

    Valley Bakery Wholesalers Inc is recalling Large Hamburger Buns because they contain egg but do not declare it on the label.

    Product
    Large Hamburger Buns, Valley Bakery, Rock Valley, IA, 12 count. UPC 290707404002, packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Food)·F-2121-2017·2017-05-03

    Valley Bakery Wheat Tea Rolls Recalled for Undeclared Egg Allergen

    Valley Bakery Wholesalers Inc is recalling Wheat Tea Rolls because the product contains egg but does not declare it on the label.

    Product
    Wheat Tea Rolls, Valley Bakery, Rock Valley, IA, 12 count. UPC 290219203556, packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2135-2017·2017-05-03

    Valley Bakery Specialty Crimp Recalled for Undeclared Egg Allergen

    Valley Bakery Wholesalers Inc is recalling Specialty Crimp products because they contain egg but do not declare it on the label.

    Product
    Specialty Crimp, Valley Bakery, Rock Valley, IA, 1 count. packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-2126-2017·2017-05-03

    Valley Bakery Steak Buns Recalled for Undeclared Egg Allergen

    Valley Bakery Wholesalers Inc is recalling 7 packages of Steak Buns because they contain egg but do not declare it on the label.

    Product
    Steak Buns, Valley Bakery, Rock Valley, IA, 6 count. UPC 290214603207, packaged in clear plastic bags
    Category
    Food
    Distribution
    2 states