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.

7901–7925 of 9611

  • SevereFDA (Drugs)·D-653-2014·2014-01-22

    Aidapak Recalls Vitamin B Complex Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Vitamin B Complex with C/Folic Acid tablets because they may be mislabeled as other prescription or over-the-counter medications.

    Product
    VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258016001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-529-2014·2014-01-22

    FDA Recalls Mislabeling of Propranolol HCL Tablets

    Aidapak Services is recalling 2,299 Propranolol HCL 10 mg tablets due to potential mislabeling as other medications.

    Product
    PROPRANOLOL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-602-2014·2014-01-22

    Warfarin Sodium Tablets Recalled Due to Potential Label Mixup

    Aidapak Services is recalling Warfarin Sodium 0.5 mg tablets because they may be mislabeled as Sodium Chloride 1 mg tablets.

    Product
    WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 51672402701
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-521-2014·2014-01-22

    Pramipexole Tablets Recalled for Potential Label Mixup with Tacrolimus

    Aidapak Services is recalling Pramipexole tablets that may be mislabeled as Tacrolimus capsules. The error could lead to patients taking the wrong medication.

    Product
    PRAMIPEXOLE DI-HCL Tablet, 0.25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058501
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1389-2014·2014-01-22

    Jensen's Recalls Hot Smoked Halibut Due to Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Hot Smoked Halibut because it may lack 'KEEP FROZEN' labeling and could be contaminated with Clostridium botulinum.

    Product
    Low salt, vacuum packaged, Hot Smoked Halibut was sold under brand Clippership. No product labeling was provided.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1392-2014·2014-01-22

    Jensen's Recalls Teriyaki Salmon for Missing Frozen Label and Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Alaska King Seafoods Short Strips Teriyaki salmon because it lacks a 'KEEP FROZEN' label, creating a potential risk of Clostridium botulinum contamination.

    Product
    Short Strips Teriyaki is a low salt, vacuum packaged, Hot Smoked Salmon, and it is sold under Alaska King Seafoods brand. The labels contain the following statement above or below the product name and/or ingredient statement: "***IMPORTANT KEEP FROZEN***THAW UNDER REFRIGERA
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-641-2014·2014-01-22

    FDA Recalls Mislabeled Darunavir Tablets Distributed by Aidapak Services

    Aidapak Services is recalling Darunavir tablets that may be mislabeled as Hydrocodone/Acetaminophen. The error could lead to incorrect medication administration.

    Product
    DARUNAVIR Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59676056630
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-613-2014·2014-01-22

    Mesalamine CR Capsules Recalled for Potential Label Mixup with Aspirin

    Aidapak Services is recalling Mesalamine CR capsules that may be mislabeled as Aspirin EC tablets due to a labeling error.

    Product
    MESALAMINE CR Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 54092018981
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-609-2014·2014-01-22

    FDA Recalls Hydrocodone/Acetaminophen Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Hydrocodone Bitartrate/Acetaminophen tablets because they may be mislabeled as Melatonin. The recall covers repacked drugs distributed in four western states.

    Product
    HYDROcodone BITARTRATE/ ACETAMINOPHEN Tablet, 7.5 mg/325 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 52544016201
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-519-2014·2014-01-22

    Finasteride Tablets Recalled for Potential Mislabeling as Other Medications

    Aidapak Services is recalling Finasteride 5 mg tablets that may be mislabeled as Digoxin or Phytonadione. The error poses a risk of incorrect medication administration.

    Product
    FINASTERIDE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714052201
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-720-2014·2014-01-22

    Aidapak Recalls Selegiline HCL Capsules Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Selegiline HCL 5 mg capsules because they may be mislabeled as Itraconazole 100 mg. The repacked drugs were distributed in four western states.

    Product
    SELEGILINE HCL, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67253070006
    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 (Food)·F-1395-2014·2014-01-22

    Jensen's Recalls Hot Smoked Sockeye Salmon for Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling 3,446 lbs of hot smoked sockeye salmon in Washington due to missing 'KEEP FROZEN' labels and potential Clostridium botulinum contamination.

    Product
    Hot Smoked Alaskan Sockeye Salmon is a low salt, vacuum packaged. Great Ruby Fish Co Sockeye Hot smoked salmon has no labels. ROLF'S Choice Sockeye Salmon is labeled in parts: "***ROLF'S CHOICE***SMOKED ALASKAN SOCKEYE SALMON*** Ingredients: salmon, salt, brown sugar, hard
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-494-2014·2014-01-22

    FDA Recalls Melatonin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 1 mg melatonin tablets that may be mislabeled as quetiapine fumarate or docusate sodium.

    Product
    MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 04746900466
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-545-2014·2014-01-22

    Aidapak Recalls Torsemide Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Torsemide 10 mg tablets that may be mislabeled as Mexiletine HCl 200 mg capsules.

    Product
    TORSEMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 31722053001
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-464-2014·2014-01-22

    Aidapak Recalls Calcium Carbonate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 10,819 tablets of Calcium Carbonate +D3 because they may be mislabeled as Digoxin or Amantadine HCl.

    Product
    CALCIUM CARBONATE +D3, Tablet, 600 mg/400 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904323392.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-672-2014·2014-01-22

    Pantoprazole Sodium Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Pantoprazole Sodium 20 mg tablets because they may be mislabeled as Dronedarone HCL 400 mg.

    Product
    PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175018046
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-473-2014·2014-01-22

    FDA Recalls Calcium Citrate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling calcium citrate tablets that may be mislabeled as trimethobenzamide HCL capsules.

    Product
    CALCIUM CITRATE, Tablet, 950 mg (200 MG ELEMENTAL Ca), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-619-2014·2014-01-22

    Aidapak Recalls Olanzapine Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Olanzapine 7.5 mg tablets because they may be mislabeled as Levothyroxine or Mirtazapine. The repacked drugs were distributed in four western states.

    Product
    OLANZapine Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55111016530
    Category
    Drug
    Distribution
    4 states
  • 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 (Food)·F-1399-2014·2014-01-22

    Jensen's Recalls Hot Smoked Salmon Due to Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Jack's Fish Spot Hot Smoked Cajun Atlantic Salmon because it may lack 'KEEP FROZEN' labeling, posing a risk of Clostridium botulinum contamination.

    Product
    Jack's Fish Spot Hot Smoked Cajun Atlantic is a low salt, vacuum packaged, Hot Smoked Salmon. This product is labeled in parts: "***Hot Smoked Atlantic Salmon*** INGREDIENTS: Atlantic Salmon, Salt, Brown Sugar, Spices and Natural Wood Smoke***Important: Keep Frozen. Thaw un
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-597-2014·2014-01-22

    FDA Recalls TACROLIMUS Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling TACROLIMUS Capsules, 1 mg, because they may be mislabeled as LEVOTHYROXINE SODIUM Tablets, 125 mcg.

    Product
    TACROLIMUS Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50742020801
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-522-2014·2014-01-22

    Pramipexole Tablets Recalled for Potential Mislabeling as Misoprostol

    Aidapak Services is recalling Pramipexole tablets that may be mislabeled as Misoprostol. The error could lead to patients receiving the wrong medication.

    Product
    PRAMIPEXOLE DI-HCL Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058701
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Food)·F-1337-2014·2014-01-22

    Jensen's Recalls Hot Smoked Salmon Due to Labeling and Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Savory Hot Smoked Salmon because it is not consistently labeled 'KEEP FROZEN' and has the potential to be contaminated with Clostridium botulinum.

    Product
    Savory Hot Smoked Salmon is Farmed Raised product, Low salt, vacuum packaged. Savory Smoked Salmon produced by Jensen's Smokehouse is not sold as a vacuum packaged product to the consumer. Products are shipped with "Keep Frozen" sticker on a case label. The case label st
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-575-2014·2014-01-22

    FDA Recalls Mislabeled Quetiapine Fumarate Tablets Distributed by Aidapak

    Aidapak Services is recalling Quetiapine Fumarate tablets that may be mislabeled as Simvastatin. The FDA classifies this as a Class II recall.

    Product
    QUETIAPINE FUMARATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 47335090288
    Category
    Drug
    Distribution
    4 states