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.

7576–7600 of 9611

  • ModerateFDA (Food)·F-1442-2014·2014-02-05

    LSG Food World Recalls Fu Zhou Vermicelli for Filth and Misbranding

    LSG Food World Inc. is recalling Fu Zhou Vermicelli due to filth and missing English translations. The product was distributed in New York.

    Product
    Lam Sheng Kee Fu Zhou Vermicell, Net Wt. 4.4 LB (2000 g), product is packaged in plastic bag with twelve (12) bags per carton. UPC 6949682 803360; Manufactured by LAM SHENG KEE (HK) INTERNATIONAL LIMITED RM3. 8/F, YUEXIU BLDG., 160-174 LOCKHART ROAD, WAN CHAI HK; Distributed by
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1441-2014·2014-02-05

    LSG Food World Recalls Jam-Filled Bread for Missing English Label Translation

    LSG Food World Inc. is recalling Bread Filled with Jam and Bean Paste Bread because the product labels lack English translations.

    Product
    Bread Filled with Jam, Net Wt. 420 g, product is packaged within a plastic bag with twelve (12) bags per carton.
    Category
    Food
    Distribution
    1 state
  • LowFDA (Food)·F-1440-2014·2014-02-05

    LSG Food World Recalls Bean Paste Bread for Labeling Defect

    LSG Food World Inc. is recalling Bean Paste Bread because the product label lacks an English translation. The recall covers 1,050 cartons distributed in New York.

    Product
    Bean Paste Bread, Net Wt. 420 g, product is packaged within a plastic bag with twelve (12) bags per carton.
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·011-2014·2014-02-04

    ConAgra Recalls Chicken Noodle Soup for Undeclared Wheat and Egg Allergens

    ConAgra Foods is recalling 54,673 pounds of chicken noodle soup mislabeled as chicken with rice, failing to declare wheat and egg allergens.

    Product
    Pennsylvania Firm Recalls Chicken Noodle Soup Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • HighUSDA FSIS·009-2014·2014-02-01

    House of Smoke Recalls Meat Products Due to Undeclared Soy Lecithin

    House of Smoke, Inc. is recalling approximately 144,000 pounds of meat and poultry products because they contain soy lecithin, a known allergen not declared on the label.

    Product
    House Of Smoke, Inc. — Colorado Firm Recalls Various Meat Products Due To Soy Lecithin
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-981-2014·2014-01-29

    FDA Recalls Bismuth Subsalicylate Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Bismuth Subsalicylate chewable tablets that may have been mislabeled as Irbesartan. The error could lead to patients taking the wrong medication.

    Product
    BISMUTH SUBSALICYLATE, CHEW Tablet, 262 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00603023516.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-989-2014·2014-01-29

    Aidapak Recalls Perphenazine Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling Perphenazine 16 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    PERPHENAZINE, Tablet, 16 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603506321.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-839-2014·2014-01-29

    Aidapak Recalls Escitalopram Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 5 mg Escitalopram tablets because they may have been mislabeled as Sodium Chloride tablets.

    Product
    ESCITALOPRAM, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093585001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-900-2014·2014-01-29

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Atorvastatin Calcium 10 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    ATORVASTATIN CALCIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378201577.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-959-2014·2014-01-29

    FDA Recalls Hyoscyamine Sulfate Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling 909 tablets of Hyoscyamine Sulfate SL 0.125 mg because they may have been mislabeled as other prescription drugs.

    Product
    HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574025001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-961-2014·2014-01-29

    Aidapak Recalls Loxapine Capsules Due to Potential Sertraline Labeling Error

    Aidapak Services, LLC is recalling Loxapine 5 mg capsules that may have been mislabeled as Sertraline HCL 50 mg tablets. The repacked drugs were distributed in four western states.

    Product
    LOXAPINE, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591036901.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-993-2014·2014-01-29

    FDA Recalls Propranolol HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Propranolol HCL 10 mg tablets because they may have been mislabeled as other drugs. The repacked drugs were distributed in four western states.

    Product
    PROPRANOLOL HCL, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603548221.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-928-2014·2014-01-29

    Aidapak Recalls Aspirin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 325 mg aspirin tablets because they may have been mislabeled as other prescription medications.

    Product
    ASPIRIN, Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536330501.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-850-2014·2014-01-29

    Aidapak Recalls Glyburide Tablets Due to Potential Label Mixup

    Aidapak Services is recalling glyBURIDE MICRONIZED tablets because they may have been mislabeled as digoxin. The error could lead to patients receiving the wrong medication.

    Product
    glyBURIDE MICRONIZED, Tablet, 3 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093803501.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1018-2014·2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 250 mg Ascorbic Acid tablets because they may have been mislabeled as other prescription or over-the-counter drugs.

    Product
    ASCORBIC ACID, Tablet, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052260.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-887-2014·2014-01-29

    Aidapak Recalls Rosuvastatin Calcium Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling 5 mg rosuvastatin calcium tablets because they may have been mislabeled as ibuprofen or ascorbic acid.

    Product
    ROSUVASTATIN CALCIUM, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00310075590.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1019-2014·2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 500 mg Ascorbic Acid tablets because they may have been mislabeled as Venlafaxine HCL 100 mg.

    Product
    ASCORBIC ACID, Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052372.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-938-2014·2014-01-29

    Aidapak Recalls Multivitamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling multivitamin tablets that may have been mislabeled as sitagliptin or loratadine. The FDA classifies this as a Class II recall.

    Product
    MULTIVITAMIN/MULTIMINERAL, Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536406001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-975-2014·2014-01-29

    FDA Recalls Mislabeled Quinidine Sulfate Tablets Distributed by Aidapak

    Aidapak Services, LLC is recalling Quinidine Sulfate 200 mg tablets that may have been mislabeled as Quinapril 40 mg. The error occurred during repacking in four western states.

    Product
    quiNIDine SULFATE, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591543801.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-855-2014·2014-01-29

    FDA Recalls MEXILETINE HCL Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling MEXILETINE HCL capsules because they may have been mislabeled as CALCIUM ACETATE. The error could lead to patients receiving the wrong medication.

    Product
    MEXILETINE HCL, Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093873901.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1022-2014·2014-01-29

    Aidapak Recalls Thiamine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Thiamine HCL 100 mg tablets because they may have been mislabeled as other drugs, including simvastatin and buprenorphine.

    Product
    THIAMINE HCL, Tablet, 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904054460.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-944-2014·2014-01-29

    Aidapak Recalls Niacin TR Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Niacin TR 750 mg tablets because they may have been mislabeled as Nortriptyline HCL 50 mg capsules.

    Product
    NIACIN TR, Tablet, 750 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00536703301.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0788-2014·2014-01-29

    Codman TRUFILL n-BCA Liquid Embolic System Recalled for Incorrect Instructions

    Codman & Shurtleff, Inc. is recalling 3,860 units of the TRUFILL n-BCA Liquid Embolic System due to incorrect instructions for use.

    Product
    TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System; Two 1 g tubes of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-400; The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral arteriove
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-947-2014·2014-01-29

    FDA Recalls Vitamin B Complex Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Vitamin B Complex tablets that may have been mislabeled as Cinacalcet HCl. The repacked drugs were distributed in four western states.

    Product
    VITAMIN B COMPLEX W/C, Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536730001.
    Category
    Drug
    Distribution
    4 states