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.

7626–7650 of 9611

  • SevereFDA (Drugs)·D-847-2014·2014-01-29

    Venlafaxine HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Venlafaxine HCL 100 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    VENLAFAXINE HCL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093738301.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-779-2014·2014-01-29

    FDA Recalls Potentially Mislabeled Sirolimus Tablets Distributed by Aidapak Services

    Aidapak Services is recalling 1 mg Sirolimus tablets that may be mislabeled as Propranolol or Hydrocortisone. The repacked drugs were distributed in four western states.

    Product
    SIROLIMUS, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00008104105.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-923-2014·2014-01-29

    FDA Recalls Levothyroxine Sodium Tablets Due to Potential Labeling Errors

    Aidapak Services is recalling Levothyroxine Sodium 175 mcg tablets because they may have been mislabeled as other medications.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 175 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00527135001.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-832-2014·2014-01-29

    FDA Recalls Sotalol HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Sotalol HCL 120 mg tablets because they may have been mislabeled as Neomycin Sulfate 500 mg tablets.

    Product
    SOTALOL HCL, Tablet, 120 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093106001.
    Category
    Drug
    Distribution
    4 states
  • 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
  • SevereFDA (Drugs)·D-826-2014·2014-01-29

    FDA Recalls Piroxicam Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling 10 mg Piroxicam capsules because they may have been mislabeled as Hyoscyamine Sulfate. The error could lead to patients receiving the wrong medication.

    Product
    PIROXICAM, Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093075601.
    Category
    Drug
    Distribution
    4 states
  • 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-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-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-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-867-2014·2014-01-29

    Aidapak Recalls Doxycycline Hyclate Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Doxycycline Hyclate 100 mg capsules because they may have been mislabeled as Raloxifene HCL 60 mg tablets.

    Product
    DOXYCYCLINE HYCLATE, Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00143314250.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-893-2014·2014-01-29

    FDA Recalls Tizanidine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Tizanidine HCl 2 mg tablets that may have been mislabeled as Niacin TR 500 mg.

    Product
    tiZANidine HCl, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378072219.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-898-2014·2014-01-29

    Aidapak Recalls Levothyroxine Sodium Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling Levothyroxine Sodium 112 mcg tablets because they may have been mislabeled as other drugs. The repacked drugs were distributed in four western states.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 112 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378181101.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-982-2014·2014-01-29

    FDA Recalls Mislabeled Acetaminophen, Butalbital, and Caffeine Tablets

    Aidapak Services, LLC is recalling Acetaminophen/Butalbital/Caffeine tablets that may have been mislabeled as Aspirin. The error could cause patients to take the wrong medication.

    Product
    ACETAMINOPHEN/ BUTALBITAL/ CAFFEINE, Tablet, 325 mg/50 mg/40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603254421.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-954-2014·2014-01-29

    FDA Recalls Bromocriptine Mesylate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 2.5 mg Bromocriptine Mesylate tablets because they may have been mislabeled as Benazepril HCl or Thioridazine HCl.

    Product
    BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574010603.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-786-2014·2014-01-29

    FDA Recalls Repacked Progesterone Capsules Due to Potential Labeling Error

    Aidapak Services is recalling repacked progesterone capsules that may be mislabeled as levothyroxine sodium tablets. The error could lead to patients receiving the wrong medication.

    Product
    PROGESTERONE, Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00032170801.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-992-2014·2014-01-29

    FDA Recalls Phenobarbital Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Phenobarbital tablets that may have been mislabeled as Efavirenz capsules. The error involves a label mixup during repacking.

    Product
    PHENobarbital, Tablet, 97.2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603516832.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-765-2014·2014-01-29

    Aidapak Recalls Atomoxetine Capsules Due to Potential Label Mixup

    Aidapak Services is recalling Atomoxetine HCL capsules because they may be mislabeled as other psychiatric medications.

    Product
    ATOMOXETINE HCL, Capsule, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002322930.
    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-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-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-844-2014·2014-01-29

    Losartan Potassium Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Losartan Potassium 25 mg tablets because they may have been mislabeled as Phytonadione 5 mg.

    Product
    LOSARTAN POTASSIUM, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093736498.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Drugs)·D-990-2014·2014-01-29

    FDA Recalls Phenobarbital Tablets Due to Potential Pregabalin Labeling Error

    Aidapak Services is recalling Phenobarbital tablets that may be mislabeled as Pregabalin capsules. The error poses a risk of patients receiving the wrong medication.

    Product
    PHENobarbital, Tablet, 64.8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603516721.
    Category
    Drug
    Distribution
    4 states