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.

6376–6400 of 9611

  • HighFDA (Food)·F-2397-2015·2015-06-17

    Reaction Nutrition Recalls L-Glutamine Powder for Potential Allergen Contamination

    Reaction Nutrition is recalling L-Glutamine Powder because it may contain undeclared whey protein and soy due to shared equipment use.

    Product
    RN BlueChip: Glutamine, L-Glutamine Powder, 400 grams, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2399-2015·2015-06-17

    Reaction Nutrition Recalls Pre-Workout Supplements Due to Undeclared Allergens

    Reaction Nutrition is recalling REACTION RECOR: Pre Action supplements because they may contain undeclared whey protein and soy.

    Product
    REACTION RECOR: Pre Action- 336g Orange Xplosion, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2391-2015·2015-06-17

    Reaction Nutrition Recalls Bio Armor CreaMatrix for Undeclared Allergens

    Reaction Nutrition is recalling Bio Armor CreaMatrix supplements because they may contain undeclared whey protein and soy.

    Product
    Bio Armor CreaMatrix 306g 60 servings Unflavored, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2392-2015·2015-06-17

    Reaction Nutrition Recalls Bio Armor CreaMatrix for Undeclared Allergens

    Reaction Nutrition is recalling Bio Armor CreaMatrix supplements because they may contain undeclared whey protein and soy due to shared equipment use.

    Product
    Bio Armor CreaMatrix 60 servings Blue Raspberry, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1749-2015·2015-06-17

    Orthofix Firebird Spinal Fixation System Recalled for Mislabeling

    Orthofix is recalling Firebird Spinal Fixation System screws because the length marking on the tip is incorrect.

    Product
    ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw, Standard Implant Grade Titanium Alloy Rx Only Provided Non-Sterile Do Not Reuse
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Food)·F-2420-2015·2015-06-17

    Roxy Trading Recalls Seasoning Fish Filet for Mislabeling and Missing Ingredients

    Roxy Trading Inc. is recalling Seasoning Fish Filet because the label incorrectly identifies the fish as Grouper and omits the full ingredient list.

    Product
    Seasoning Fish Filet Ingredients: Mixed Fish, Sugar, Salt, Monosodium Glutamate, Sorbic Acid Bulk cases with 12kg of fish fillets which are packaged in clear plastic. The label does not declare the type of fish, other ingredients in the product, or nutrition facts.
    Category
    Food
    Distribution
    0 states
  • ModerateFDA (Food)·F-2405-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid, 50ml, because the outside packaging may have incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid, 50ml
    Category
    Drug
    Distribution
    37 states
  • ModerateFDA (Devices)·Z-1717-2015·2015-06-17

    Extentrac Elite Powered Decompression Table Recalled for Weight Limit Mislabeling

    Advanced Back Technologies is recalling 36 Extentrac Elite powered decompression tables because the product brochure incorrectly states a 350-lb weight limit, while the device is only approved for patients up to 300 lbs.

    Product
    Extentrac Elite product brochure DCN: 13-001, 09-001 (Powered decompression table, for traction)
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Food)·F-2406-2015·2015-06-17

    Rugby Poly Vitamin Liquid Recalled for Packaging Label Mismatch

    Pharmatech LLC is recalling Rugby Poly Vitamin Liquid with Iron because the outside packaging labels may not match the individual product labeling, potentially displaying incorrect lot, expiration, or product identity information.

    Product
    Rugby Poly Vitamin Liquid with Iron, 50 ml
    Category
    Drug
    Distribution
    37 states
  • ModerateUSDA FSIS·093-2015·2015-06-17

    Pinnacle Foods Recalls Swanson Turkey Dinners for Undeclared MSG

    Pinnacle Foods is recalling approximately 668,316 pounds of Swanson Stuffing Baked Turkey dinners because the product contains monosodium glutamate (MSG) that is not declared on the label.

    Product
    Recall Notification Report 093-2015 (Poultry Products )
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1718-2015·2015-06-17

    Advanced Back Technologies Recalls Extentrac Elite User Manual

    Advanced Back Technologies is recalling 18 Extentrac Elite User Manuals because they incorrectly state the device is for patients up to 350 lbs, while the device is only approved for up to 300 lbs.

    Product
    Extentrac Elite User Manual DCN: 14-001 (Powered decompression table, for traction)
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-1133-2015·2015-06-17

    SCA Pharmaceuticals Recalls Phenylephrine Bags Due to Labeling Error

    SCA Pharmaceuticals is recalling 50 bags of phenylephrine HCl 50 mg in 0.9% sodium chloride due to a label mix-up. The product was incorrectly labeled instead of phenylephrine in 5% dextrose.

    Product
    PHENYLephrine HCl 50 mg in 0.9% Sodium Chloride 250 mL bag (Concentration = 0.2 mg per mL), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR (877) 550-5059, barcode 88888772029.
    Category
    Drug
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-1132-2015·2015-06-17

    Mallinckrodt Recalls MD Gastroview Due to Labeling Errors

    Mallinckrodt is recalling 6,600 bottles of MD Gastroview because some bottles have incorrect or missing lot numbers and expiration dates.

    Product
    MD GASTROVIEW — MD GASTROVIEW (DIATRIZOATE MEGLUMINE AND DIATRIZOATE SODIUM)
    Category
    Drug
    Distribution
    0 states
  • LowFDA (Devices)·Z-1755-2015·2015-06-17

    Biomet Shoulder Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet, Inc. is recalling specific shoulder joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma. Shoulder joint replacement components include humeral stems, humeral heads, and glenoid components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1754-2015·2015-06-17

    Biomet Recalls Hip Components Due to Incorrect GTIN Labeling Codes

    Biomet is recalling specific hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma Uncemented, & Mallory/Head Total Hip System Size 12, 165 mm, Bi- Metric Femoral Components. Hip joint replacement components include: femoral stems, femoral heads, acetabular sh
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1756-2015·2015-06-17

    Biomet Knee Joint Replacement Components Recalled for Incorrect GTIN Codes

    Biomet is recalling MCK Maximum Congruent Knee System components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint replacement prostheses components include femoral, tibial, and patellar components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1757-2015·2015-06-17

    Biomet Recalls Hip Joint Components Due to Incorrect GTIN Labeling

    Biomet is recalling 1,315 hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.

    Product
    Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD +6MM NO SKIRT Hip joint replacement components include: femoral stems, femoral heads, acetabular
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·092-2015·2015-06-16

    Venus Foods Recalls Pork Sausage for Undeclared Wheat Allergen

    Venus Foods Inc. is recalling approximately 25,380 pounds of pork sausage products because they contain wheat, a known allergen, that is not declared on the label.

    Product
    Venus Foods Inc. — Venus Foods Inc Recalls Pork Sausage Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-2403-2015·2015-06-10

    Ava's Berry Nutty Mix Recalled for Undeclared Sulfites

    Northhampton Peanut Company is recalling Ava's Berry Nutty Mix trail mix because it contains undeclared sulfites.

    Product
    Ava's Berry Nutty Mix trail mix packed in 20 oz. clear plastic containers.
    Category
    Food
    Distribution
    5 states