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.

7751–7775 of 9611

  • ModerateFDA (Drugs)·D-821-2014·2014-01-29

    Desloratadine Tablets Recalled for Potential Labeling Mixup

    Aidapak Services, LLC is recalling Desloratadine 5 mg tablets due to a potential label mixup with Ascorbic Acid 250 mg tablets.

    Product
    DESLORATADINE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00085126401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-932-2014·2014-01-29

    Aidapak Recalls Mislabeled Cyanocobalamin Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling 500 mcg Cyanocobalamin tablets that were mislabeled as Sevelamer Carbonate or other drugs. The recall covers products distributed in Arizona, California, Oregon, and Washington.

    Product
    CYANOCOBALAMIN, Tablet, 500 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536355101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-805-2014·2014-01-29

    Pregabalin Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Pregabalin 25 mg capsules because they may have been mislabeled as Cholecalciferol or Glyburide.

    Product
    PREGABALIN, Capsule, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071101268.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-985-2014·2014-01-29

    Methylprednisolone Tablets Recalled for Potential Labeling Mixup

    Aidapak Services, LLC is recalling methylprednisolone tablets that may have been mislabeled as omeprazole/sodium bicarbonate capsules.

    Product
    methylPREDNISolone, Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603459321.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-843-2014·2014-01-29

    Aidapak Recalls Mislabeled Amlodipine Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling 5 mg amlodipine besylate tablets that may have been mislabeled as cyanocobalamin. The error involves a label mixup affecting specific lots.

    Product
    amLODIPine BESYLATE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093716798.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0820-2014·2014-01-29

    FDA Recalls Composix L/P Mesh Due to Labeling Mismatch

    Davol, Inc. is recalling 46 units of Composix L/P Mesh with Echo PS Positioning System because the product labeling does not match the product configuration.

    Product
    Composix L/P with Echo PS 6" X 8" Product Code 0144680 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the reconstruction o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-807-2014·2014-01-29

    Aidapak Recalls Phenytoin Sodium ER Capsules Due to Labeling Error

    Aidapak Services is recalling Phenytoin Sodium ER capsules because they may have been mislabeled as Lithium Carbonate ER tablets.

    Product
    PHENYTOIN SODIUM ER, Capsule, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071374066.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1001-2014·2014-01-29

    Aidapak Recalls Isosorbide Dinitrate Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling Isosorbide Dinitrate 5 mg tablets that may have been mislabeled as Cilostazol or Perphenazine.

    Product
    ISOSORBIDE DINITRATE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781163501.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-829-2014·2014-01-29

    Aidapak Recalls Nortriptyline Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Nortriptyline HCL capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.

    Product
    NORTRIPTYLINE HCL, Capsule, 75 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093081301.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-931-2014·2014-01-29

    Aidapak Recalls Cyanocobalamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 100 mcg cyanocobalamin tablets because they may have been mislabeled as guaiFENesin ER 600 mg tablets.

    Product
    CYANOCOBALAMIN, Tablet, 100 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536354201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-767-2014·2014-01-29

    Aidapak Recalls Atomoxetine Capsules Due to Potential Lovastatin Label Mixup

    Aidapak Services is recalling Atomoxetine HCL capsules because they may be mislabeled as Lovastatin tablets. The repacked drugs were distributed in four western states.

    Product
    ATOMOXETINE HCL, Capsule, 18 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002323830.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0803-2014·2014-01-29

    Civco Belly Board MRI Recalled Due to Misaligned Scales

    Civco Medical Instruments is recalling specific lots of Belly Board MRI devices because scales may be misaligned, potentially affecting measurement accuracy.

    Product
    Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cushion, REF 126000, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-986-2014·2014-01-29

    Aidapak Recalls Modafinil Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Modafinil 200 mg tablets because they may have been mislabeled as Omega-3-Acid Ethyl Esters capsules.

    Product
    MODAFINIL, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603466216.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-945-2014·2014-01-29

    Aidapak Recalls Niacin TR Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Niacin TR 1000 mg tablets because they may have been mislabeled as 750 mg tablets. The repacked drugs were distributed in four western states.

    Product
    NIACIN TR, Tablet, 1000 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00536703801.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1013-2014·2014-01-29

    Aidapak Recalls Amantadine HCL Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Amantadine HCL 100 mg tablets because they may have been mislabeled as other medications.

    Product
    AMANTADINE HCL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00832011100.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-769-2014·2014-01-29

    Raloxifene HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Raloxifene HCL tablets due to a potential label mixup with Isosorbide Mononitrate.

    Product
    RALOXIFENE HCL, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002416530.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-777-2014·2014-01-29

    Carvedilol Phosphate ER Capsules Recalled for Potential Labeling Error

    Aidapak Services is recalling Carvedilol Phosphate ER capsules due to a potential label mixup with Bumetanide tablets.

    Product
    CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00007337113.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-918-2014·2014-01-29

    Sodium Chloride Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling 1,000 mg sodium chloride tablets that may be mislabeled as repaglinide. The error involves specific lots distributed in four western states.

    Product
    SODIUM CHLORIDE, Tablet, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00527111610
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-899-2014·2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Levothyroxine Sodium tablets that may have been mislabeled as Pramipexole Di-HCl.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 175 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378181701
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-905-2014·2014-01-29

    Temazepam Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Temazepam 7.5 mg capsules because they may be mislabeled as Calcium Citrate or Valsartan.

    Product
    TEMAZEPAM, Capsule, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378311001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1023-2014·2014-01-29

    Aidapak Recalls Niacin TR Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Niacin TR capsules because they may have been mislabeled as Methylergonovine Maleate tablets.

    Product
    NIACIN TR, Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904062960.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-877-2014·2014-01-29

    Midodrine HCL Tablets Recalled for Potential Labeling Error

    Aidapak Services, LLC is recalling Midodrine HCL 2.5 mg tablets that may have been mislabeled as Pioglitazone HCL 15 mg.

    Product
    MIDODRINE HCL, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185004001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-936-2014·2014-01-29

    Aidapak Recalls Docusate Sodium Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 16,044 Docusate Sodium capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.

    Product
    DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536375710.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-876-2014·2014-01-29

    Aidapak Recalls Sennosides Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Sennosides tablets because they may have been mislabeled as other medications. The recall covers distribution in four western states.

    Product
    SENNOSIDES, Tablet, 8.6 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00182109301.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-793-2014·2014-01-29

    Aidapak Recalls Exemestane Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Exemestane 25 mg tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.

    Product
    EXEMESTANE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054008013.
    Category
    Drug
    Distribution
    4 states