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.

7851–7875 of 9611

  • ModerateFDA (Drugs)·D-825-2014·2014-01-29

    Aidapak Recalls Metoprolol Tartrate Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 50 mg metoprolol tartrate tablets because they may have been mislabeled as other medications.

    Product
    METOPROLOL TARTRATE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093073301.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-924-2014·2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Levothyroxine Sodium tablets that may have been mislabeled as Isoniazid due to a labeling error.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 137 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00527163801.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-963-2014·2014-01-29

    Aidapak Recalls Estropipate Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Estropipate 0.75 mg tablets because they may have been mislabeled as Mesalamine DR 400 mg capsules.

    Product
    ESTROPIPATE, Tablet, 0.75 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591041401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-778-2014·2014-01-29

    Aidapak Recalls Mislabeled Pantoprazole Sodium DR Tablets

    Aidapak Services is recalling 20 mg Pantoprazole Sodium DR tablets because they may be mislabeled as Hyoscyamine Sulfate or Multivitamin/Multimineral.

    Product
    PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00008060601.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-831-2014·2014-01-29

    Aidapak Recalls Nefazodone 200 mg Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Nefazodone HCL 200 mg tablets because they may have been mislabeled as 150 mg tablets.

    Product
    NEFAZODONE HCL, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093102506.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1009-2014·2014-01-29

    Aidapak Recalls Levothyroxine Sodium Tablets Due to Labeling Errors

    Aidapak Services is recalling Levothyroxine Sodium tablets because they may have been mislabeled as other prescription drugs.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 88 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781518392.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-774-2014·2014-01-29

    SitaGLIPtin Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling sitaGLIPtin phosphate tablets because they may be mislabeled as Lactobacillus or Cyanocobalamin.

    Product
    sitaGLIPtin PHOSPHATE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00006011231.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1010-2014·2014-01-29

    FDA Recalls Levothyroxine Sodium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Levothyroxine Sodium tablets that may have been mislabeled as Omega-3 Fatty Acid capsules.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 137 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781519192.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-930-2014·2014-01-29

    Aidapak Recalls Multivitamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling specific lots of multivitamin chew tablets because they may have been mislabeled as other drugs.

    Product
    MULTIVITAMIN/MULTIMINERAL, CHEW Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536344308.
    Category
    Drug
    Distribution
    4 states
  • LowFDA (Devices)·Z-0801-2014·2014-01-29

    Philips CT Scanner Recall for Obscured Machine Name Label

    Philips is recalling 32 CT scanners because the machine name label is obscured in TumorLOC Basic Mode, preventing users from viewing or changing the name.

    Product
    Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Brilliance CT Big Bore Radiology) Distributed by Philips Healthcare System, Cleveland, OH. Produces cross-sectional body images by computer reconstruction of x-ray transmission data taken at different angles a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0821-2014·2014-01-29

    Puritan Bennett Ventilator Manual Addendum Corrected for Oxygen Sensor Life

    Nellcor Puritan Bennett is correcting a labeling error in the PB840 Operator's Manual Addendum that incorrectly stated the oxygen sensor life as two years instead of one.

    Product
    Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of the oxygen sensor is to provide the oxygen concentration of the delivered gas at the patient wye (inspiratory-expiratory interface). The oxygen sensor does not control t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0789-2014·2014-01-29

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

    Codman & Shurtleff, Inc. is recalling 7,983 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: One 1 g tube of n-BCA, one 10 mL vial of Ethiodized Oil and one 1 g vial of Tantalum Powder Product Code: 631-500 The TRUFILL n-BCA Liquid Embolic System is indicated for the embolization of cerebral arterioveno
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·007-2014·2014-01-27

    George's Recalls Frozen Chicken Products Due to Undeclared Wheat Allergen

    George's Inc. is recalling approximately 1.25 million pounds of frozen chicken products because wheat, a known allergen, was not declared on the labels.

    Product
    George's Further Processing — Arkansas Firm Recalls Frozen Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-582-2014·2014-01-22

    Aspirin Tablets Recalled for Potential Mislabeling as Cholecalciferol

    Aidapak Services is recalling Aspirin tablets that may be mislabeled as Cholecalciferol. The FDA classifies this as a Class II recall.

    Product
    ASPIRIN Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348000123
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-510-2014·2014-01-22

    Aidapak Recalls Mislabeled Pantoprazole Sodium Tablets

    Aidapak Services, LLC is recalling 20 mg pantoprazole sodium tablets that may be mislabeled as nortriptyline hydrochloride capsules.

    Product
    PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13668009690
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-608-2014·2014-01-22

    FDA Recalls FIDAXOMICIN Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling FIDAXOMICIN 200 mg tablets that may be mislabeled as BENAZEPRIL HCL 40 mg. The error affects repacked drugs distributed in four western states.

    Product
    FIDAXOMICIN Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 52015008001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-673-2014·2014-01-22

    Aidapak Recalls OXcarbazepine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling OXcarbazepine 150 mg tablets because they may be mislabeled as traZODone HCl 50 mg.

    Product
    OXcarbazepine Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018388
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-704-2014·2014-01-22

    Sodium Bicarbonate Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling 1,013 sodium bicarbonate tablets that may be mislabeled as nicotine polacrilex lozenges.

    Product
    SODIUM BICARBONATE Tablet, 650 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980018210
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-644-2014·2014-01-22

    Aidapak Recalls Nifedipine Capsules Due to Potential Labeling Error

    Aidapak Services is recalling Nifedipine 10 mg capsules because they may be mislabeled as Nitrofurantoin 100 mg. The repacked drugs were distributed in four western states.

    Product
    NIFEdipine Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762100401
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-474-2014·2014-01-22

    Calcium Citrate Tablets Recalled for Potential Lithium Carbonate Labeling Error

    Aidapak Services is recalling Calcium Citrate tablets that may be mislabeled as Lithium Carbonate ER. The error could lead to incorrect medication administration.

    Product
    CALCIUM CITRATE, Tablet, 950 mg (200 mg Elemental Calcium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-689-2014·2014-01-22

    Aidapak Recalls Mislabeled Pantoprazole Sodium Tablets

    Aidapak Services, LLC is recalling 20 mg Pantoprazole Sodium tablets that may be mislabeled as Fosinopril Sodium. The error involves a label mixup on repacked drugs.

    Product
    PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043304
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-484-2014·2014-01-22

    FDA Recalls Glucosamine/Chondroitin Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Glucosamine/Chondroitin DS tablets because they may be mislabeled as Docusate Sodium capsules. The error could lead to patients taking the wrong medication.

    Product
    GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904559293
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-600-2014·2014-01-22

    Aidapak Recalls Clomipramine Capsules Due to Potential Labeling Errors

    Aidapak Services is recalling Clomipramine HCl capsules because they may be mislabeled as other prescription medications.

    Product
    clomiPRAMINE HCl Capsule, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672401205
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-579-2014·2014-01-22

    Aidapak Recalls Lactobacillus GG Capsules Due to Labeling Mixup

    Aidapak Services is recalling Lactobillus GG capsules because they may be mislabeled as other medications, including Tacrolimus.

    Product
    LACTOBACILLUS GG Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49100036374
    Category
    Drug
    Distribution
    4 states