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.

7926–7950 of 9611

  • 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-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 (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-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 (Food)·F-1398-2014·2014-01-22

    Jensen's Recalls Hot Smoked Salmon Due to Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling Jack's Fish Spot Hot Smoked Atlantic Garlic & Pepper Chunks because the product may lack 'KEEP FROZEN' labeling and could be contaminated with Clostridium botulinum.

    Product
    Jack's Fish Spot Hot Smoked Atlantic Garlic & Pepper Chunks is a low salt, vacuum packaged, hot smoked salmon. The product is labeled in parts: "***Hot Smoked Atlantic Salmon*** INGREDIENTS: Atlantic Salmon, Salt, Brown Sugar, Spices and Natural Wood Smoke***Important: Keep
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1397-2014·2014-01-22

    Jensen's Alaska King Salmon Garlic Pepper Hot Smoked Salmon Recall

    Jensen's Old Fashioned Smokehouse is recalling Garlic Pepper Hot Smoked Salmon due to missing 'KEEP FROZEN' labels and potential Clostridium botulinum contamination.

    Product
    Low salt, vacuum packaged, Garlic Pepper Hot Smoked Salmon with Hardwood. AKS (Alaska King Salmon) product is labeled in parts: "***Garlic Pepper Smoked Salmon product ***GARLIC PEPPER SMOKED SALMON ***INGREDIENTS: SALMON, SALT, BROWN SUGAR, GARLIC, PEPPER, HARDWOOD SMOKE***"
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-675-2014·2014-01-22

    Letrozole Tablets Recalled for Potential Mislabeling as Metoprolol Tartrate

    Aidapak Services, LLC is recalling Letrozole 2.5 mg tablets that may be mislabeled as Metoprolol Tartrate 50 mg. The error could lead to patients receiving the wrong medication.

    Product
    LETROZOLE Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756051183
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-723-2014·2014-01-22

    FDA Recalls Mislabelled Ibuprofen Tablets Distributed by Aidapak Services

    Aidapak Services is recalling 400 mg ibuprofen tablets that may be mislabeled as 325 mg aspirin. The repacked drugs were distributed in four western states.

    Product
    IBUPROFEN, Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67877029401
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Food)·F-1394-2014·2014-01-22

    Jensen's Recalls Hot Smoked Pink Salmon for Botulism Risk

    Jensen's Old Fashioned Smokehouse is recalling 20,271 lbs of Hot Smoked Pink Salmon in Washington due to missing 'KEEP FROZEN' labels and potential Clostridium botulinum contamination.

    Product
    Hot Smoked Pink Salmon is Low salt, vacuum packaged. Clippership Hot Smoked Pink Salmon does not have any labels. Lummi Island Co-Op product's label is read in parts: "***WILD SMOKED PINK SALMON***LUMMI ISLANDWILD.COM***KEEP FROZEN***Thawing Instructions: Remove all packag
    Category
    Food
    Distribution
    1 state
  • HighFDA (Drugs)·D-671-2014·2014-01-22

    Aidapak Recalls Isosorbide Mononitrate Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Isosorbide Mononitrate ER tablets because they may be mislabeled as other prescription drugs.

    Product
    ISOSORBIDE MONONITRATE ER Tablet, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175012837
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-508-2014·2014-01-22

    Aidapak Recalls Labeled LamoTRIgine Tablets Due to Potential Label Mixup

    Aidapak Services is recalling lamoTRIgine tablets that may be mislabeled as oxybutynin chloride or fexofenadine HCL. The error could lead to patients taking the wrong medication.

    Product
    lamoTRIgine, Tablet, 50 mg (1/2 of 100 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 13668004701
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-557-2014·2014-01-22

    Liothyronine Sodium Tablets Recalled for Potential Labeling Errors

    Aidapak Services is recalling Liothyronine Sodium 25 mcg tablets because they may be mislabeled as Guanfacine or Bromocriptine.

    Product
    LIOTHYRONINE SODIUM, Tablet 25 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 42794001902
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-518-2014·2014-01-22

    FDA Recalls Famotidine Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling 700-tablet bottles of 20 mg Famotidine tablets because they may be mislabeled as other medications.

    Product
    FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-569-2014·2014-01-22

    Aidapak Recalls GuaiFENesin ER Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling guaiFENesin ER tablets because they may be mislabeled as fenofibrate or glyburide. The error poses a risk of patients taking the wrong medication.

    Product
    guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45802049878
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-465-2014·2014-01-22

    Aidapak Recalls Omega-3 Fatty Acid Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling 2,799 Omega-3 Fatty Acid capsules because they may be mislabeled as Docusate Calcium. The error could lead to patients receiving the wrong medication.

    Product
    OMEGA-3 FATTY ACID, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904404360
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Food)·F-1387-2014·2014-01-22

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

    Jensen's Old Fashioned Smokehouse is recalling hot smoked salmon because inconsistent 'KEEP FROZEN' labeling creates a potential risk of Clostridium botulinum contamination.

    Product
    Low salt, vacuum packaged, Hot Smoked Farmed Raised Salmon (Atlantic, Coho, Keta, King, Steelhead, and Sockeye). AKS (Alaska King Seafoods) products such as Sockeye Traditional, Coho Traditional, Keta Traditional, Farmed Atlantic Traditional are labeled in parts: "***IMPORTAN
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1404-2014·2014-01-22

    Concertos In Chocolate Recalls Solid Milk Chocolate Santa Candy

    Concertos In Chocolate LLC is recalling Solid Milk Chocolate Santa candy because it is incorrectly labeled and contains an undeclared milk allergen.

    Product
    SOLID MILK CHOCOLATE SANTA candy
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-491-2014·2014-01-22

    Aidapak Recalls Docusate Sodium Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 4,318 Docusate Sodium capsules because they may be mislabeled as other medications. The repacked drugs were distributed in Arizona, California, Oregon, and Washington.

    Product
    DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904789159
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-550-2014·2014-01-22

    Nicotine Polacrilex Lozenges Recalled for Potential Label Mixup

    Aidapak Services is recalling 1,582 Nicotine Polacrilex Lozenges because they may be mislabeled as other prescription drugs.

    Product
    NICOTINE POLACRILEX Lozenge, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 37205098769
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-691-2014·2014-01-22

    Zolpidem Tartrate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Zolpidem Tartrate tablets that may be mislabeled as Temazepam capsules due to a label mixup.

    Product
    ZOLPIDEM TARTRATE, Tablet, 2.5 mg (1/2 of 5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 64679071401
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-642-2014·2014-01-22

    Methylprednisolone Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling methylprednisolone tablets that may be mislabeled as levothyroxine sodium due to a labeling mixup.

    Product
    methylPREDNISolone Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59746000103
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-639-2014·2014-01-22

    Aripiprazole Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Aripiprazole 2 mg tablets because they may be mislabeled as other prescription drugs.

    Product
    ARIPiprazole Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59148000613
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-731-2014·2014-01-22

    FDA Recalls Pramipexole Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Pramipexole Di-HCl tablets that may be mislabeled as Liothyronine Sodium. The error poses a risk of incorrect medication administration.

    Product
    PRAMIPEXOLE DI-HCL, Tablet, 1.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462033490
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-645-2014·2014-01-22

    Aidapak Recalls Mirtazapine Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Mirtazapine 7.5 mg tablets because they may be mislabeled as other prescription medications.

    Product
    MIRTAZAPINE Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762141503
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-527-2014·2014-01-22

    Leflunomide Tablets Recalled Due to Potential Labeling Mixup

    Aidapak Services is recalling Leflunomide 10 mg tablets because they may be mislabeled as Doxycycline or Sevelamer Carbonate.

    Product
    LEFLUNOMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155004303
    Category
    Drug
    Distribution
    4 states