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.

7951–7975 of 9611

  • ModerateFDA (Drugs)·D-564-2014·2014-01-22

    Misoprostol Tablets Recalled for Potential Labeling Error

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

    Product
    MISOPROSTOL Tablet, 100 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386016012
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-663-2014·2014-01-22

    Olanzapine Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Olanzapine 7.5 mg tablets due to a potential labeling mixup with Nortriptyline HCL capsules.

    Product
    OLANZAPINE, Tablet 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505311203
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-709-2014·2014-01-22

    Aidapak Multivitamin Tablets Recalled for Potential Prenatal Label Mixup

    Aidapak Services is recalling Multivitamin/Multimineral Tablets due to a labeling error where they may be mislabeled as Prenatal Multivitamin/Multimineral Tablets.

    Product
    MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066810
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-713-2014·2014-01-22

    Aidapak Recalls Benazepril HCL Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 799 Benazepril HCL tablets because they may be mislabeled as other medications.

    Product
    BENAZEPRIL HCL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075410
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-683-2014·2014-01-22

    Aidapak Recalls GuaiFENesin ER Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling guaiFENesin ER tablets because they may be mislabeled as prenatal multivitamin or other medications.

    Product
    guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-504-2014·2014-01-22

    FDA Recalls Omeprazole Capsules Due to Potential Labeling Mixup

    Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Lactobacillus GG or Pyridoxine HCL.

    Product
    OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1110 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-479-2014·2014-01-22

    FDA Recalls Zinc Sulfate Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Zinc Sulfate capsules that may be mislabeled as Phosphorus tablets. The error involves a label mixup on repacked products.

    Product
    ZINC SULFATE, Capsule, 220 mg (50 mg Elem Zn), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904533260
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-695-2014·2014-01-22

    Aidapak Recalls Hydrocortisone Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Hydrocortisone 5 mg tablets that may be mislabeled as Orphenadrine Citrate ER or Calcium Acetate.

    Product
    HYDROCORTISONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64720033105
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-716-2014·2014-01-22

    Aidapak Recalls Quetiapine Fumarate Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Quetiapine Fumarate 25 mg tablets because they may be mislabeled as Chlordiazepoxide HCl capsules.

    Product
    QUEtiapine FUMARATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862048901
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-661-2014·2014-01-22

    Aidapak Recalls Atorvastatin Calcium Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Atorvastatin Calcium 20 mg tablets because they may be mislabeled as GuaiFENesin ER 600 mg.

    Product
    ATORVASTATIN CALCIUM Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505257909
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-500-2014·2014-01-22

    Aidapak Recalls Niacin TR Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Niacin TR tablets because they may be mislabeled as Solifenacin Succinate.

    Product
    NIACIN TR, Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10939043533
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-562-2014·2014-01-22

    Lactobacillus Acidophilus Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Lactobacillus Acidophilus capsules because they may be mislabeled as Docusate Sodium. Consumers should stop using the product.

    Product
    LACTOBACILLUS ACIDOPHILUS Capsule, 500 Million CFU, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 43292055746
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0768-2014·2014-01-22

    Anspach Micro Curved Attachment Cutting Burrs Recalled for Labeling Issues

    The Anspach Effort, Inc. is recalling all lots of MCA Cutting Burrs and Dissection Tools because the indications for use were broader than validated and directions were unclear.

    Product
    MCA7-2SB - 2MM Fluted Ball, 7.3CM. All lots are included in recall. Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-734-2014·2014-01-22

    Aidapak Recalls Melatonin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 1 mg Melatonin tablets that may be mislabeled as Omega-3 fatty acid capsules. The error involves a potential mix-up between two different products.

    Product
    MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 74312002832
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-604-2014·2014-01-22

    Carbamazepine ER Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling carbamazepine ER tablets that may be mislabeled as acarbose due to a label mixup.

    Product
    carBAMazepine ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672412401
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0749-2014·2014-01-22

    Anspach Micro Curved Cutting Burrs Recalled for Labeling Errors

    The Anspach Effort, Inc. is recalling Micro Curved Attachment Cutting Burrs because the indications for use were broader than validated and directions were unclear.

    Product
    Micro Curved Attachment (MCA) Cutting Burr, DFU 18-0001. All lots are included in recall. Part Number MCA Intended for use in cutting and shaping delicate bone material, primarily in otologic procedures such as cochleostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-503-2014·2014-01-22

    FDA Recalls Omeprazole Capsules Due to Potential Labeling Mixup

    Aidapak Services is recalling Omeprazole/Sodium Bicarbonate capsules because they may be mislabeled as Benzocaine/Menthol lozenges. The FDA classifies this as a Class II recall.

    Product
    OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/110 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-475-2014·2014-01-22

    FDA Recalls Pseudoephedrine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Pseudoephedrine HCL 60 mg tablets because they may be mislabeled as Repaglinide 1 mg tablets.

    Product
    PSEUDOEPHEDRINE HCL, Tablet, 60 mg, Rx in Oregon, Distributed by: AidaPak Service, LLC, NDC 00904512559
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-706-2014·2014-01-22

    Aidapak Recalls Folic Acid Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling 1 mg Folic Acid tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    FOLIC ACID, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162036110
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-566-2014·2014-01-22

    FDA Recalls Orphenadrine Citrate Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Orphenadrine Citrate ER tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.

    Product
    ORPHENADRINE CITRATE ER Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386048024
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-592-2014·2014-01-22

    Aidapak Recalls Trazodone Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Trazodone HCl 50 mg tablets because they may be mislabeled as Dexamethasone, Docusate Sodium, or Guanfacine.

    Product
    traZODone HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111043301
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-690-2014·2014-01-22

    Aidapak Recalls 40 mg Pantoprazole Sodium Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling 1,001 tablets of 40 mg Pantoprazole Sodium due to a potential labeling mixup with Sennosides.

    Product
    PANTOPRAZOLE SODIUM DR Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043402
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-534-2014·2014-01-22

    Venlafaxine HCL Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Venlafaxine HCL 50 mg tablets because they may be mislabeled as sulfasalazine 500 mg.

    Product
    VENLAFAXINE HCL Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155024801
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-724-2014·2014-01-22

    Aidapak Recalls Quinapril HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 20 mg Quinapril HCL tablets because they may be mislabeled as Multivitamin/Multimineral tablets.

    Product
    QUINAPRIL HCL, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68180055809
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Food)·F-1396-2014·2014-01-22

    Jensen's Recalls Unlabeled Hot Smoked Salmon Products

    Jensen's Old Fashioned Smokehouse is recalling Great Ruby Fish Co. and Rolf's Choice hot smoked salmon products that lack 'KEEP FROZEN' labels.

    Product
    Great Ruby Fish Co products are such as Keta and King Hot smoked salmon. No labels provided. Products are labeled with lot code sticker and "KEEP FROZEN" sticker on individual units. The customer applies their own label upon receipt. Rolf's Choice Sockeye hot smoked salmon
    Category
    Food
    Distribution
    1 state