The Recall Desk

Severity 2 of 5

Moderate recalls

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

What “moderate” means here

Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

19126–19150 of 21751

  • ModerateFDA (Drugs)·D-830-2014·2014-01-29

    Aidapak Recalls Clonazepam Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling clonazepam 0.25 mg tablets that may have been mislabeled as cholecalciferol 2000 units capsules.

    Product
    clonazePAM, Tablet, 0.25 mg (1/2 of 0.5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00093083201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-858-2014·2014-01-29

    Acyclovir Tablets Recalled Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Acyclovir 800 mg tablets that may have been mislabeled as Pantoprazole Sodium 20 mg.

    Product
    ACYCLOVIR, Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093894701.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-920-2014·2014-01-29

    Aidapak Recalls Levothyroxine Sodium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Levothyroxine Sodium tablets because they may have been mislabeled as other prescription drugs.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00527134101.
    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-995-2014·2014-01-29

    Aidapak Recalls Perphenazine Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Perphenazine 8 mg tablets that may have been mislabeled as Nifedipine 10 mg capsules.

    Product
    PERPHENAZINE, Tablet, 8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00630506221.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1011-2014·2014-01-29

    Bromocriptine Mesylate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Bromocriptine Mesylate 2.5 mg tablets because they may have been mislabeled as Cyanocobalamin 1000 mcg.

    Product
    BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781532531.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-848-2014·2014-01-29

    Venlafaxine HCL ER Capsules Recalled for Potential Label Mixup

    Aidapak Services is recalling Venlafaxine HCL ER capsules due to a potential label mixup with other medications. The repacked drugs were distributed in four western states.

    Product
    VENLAFAXINE HCL ER, Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093738656.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0802-2014·2014-01-29

    Civco Belly Board Recalled Due to Misaligned Scales

    Civco Medical Instruments is recalling 138 belly boards because scales may be misaligned from the zero reference, potentially affecting measurement accuracy.

    Product
    Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, 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-968-2014·2014-01-29

    Desmopressin Acetate Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Desmopressin Acetate tablets because they may have been mislabeled as Loxapine capsules.

    Product
    DESMOPRESSIN ACETATE, Tablet 0.1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591246401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-803-2014·2014-01-29

    Aidapak Recalls Varenicline Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Varenicline 0.5 mg tablets because they may have been mislabeled as other prescription drugs. The recall covers specific lots distributed in four western states.

    Product
    VARENICLINE, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00069046856.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1016-2014·2014-01-29

    Aidapak Recalls Vitamin B Complex Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Vitamin B Complex tablets because they may have been mislabeled as other drugs. The repacked products were distributed in four western states.

    Product
    VITAMIN B COMPLEX W/C, Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904026013.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-980-2014·2014-01-29

    Aidapak Recalls Aspirin/ER Dipyridamole Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Aspirin/ER Dipyridamole capsules because they may have been mislabeled as other medications.

    Product
    ASPIRIN/ER DIPYRIDAMOLE, Capsule, 25 mg/200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00597000160.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-890-2014·2014-01-29

    Aidapak Recalls Chlorthalidone Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Chlorthalidone 12.5 mg tablets because they may have been mislabeled as Propranolol HCl 5 mg tablets.

    Product
    CHLORTHALIDONE, Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00378022201.
    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-872-2014·2014-01-29

    Aidapak Recalls Dutasteride Capsules Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling 0.5 mg Dutasteride capsules because they may have been mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    DUTASTERIDE, Capsule, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00173071204.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-927-2014·2014-01-29

    Aidapak Recalls Aspirin Chew Tablets Due to Potential Label Mixup

    Aidapak Services is recalling 81 mg aspirin chew tablets because they may have been mislabeled as other medications, including modafinil and omega-3 fatty acids.

    Product
    ASPIRIN, CHEW Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536329736.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-799-2014·2014-01-29

    Aidapak Recalls Mercaptopurine Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling 50 mg Mercaptopurine tablets because they may have been mislabeled as 500 mg Ascorbic Acid tablets.

    Product
    MERCapsuleTOPURINE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054458111.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0794-2014·2014-01-29

    Remel Recalls Oxoid Ampicillin Test Discs Due to Missing Antibiotic

    Remel Inc is recalling 80 packs of Oxoid Ampicillin 10 mcg test discs because some cartridges may contain discs not impregnated with antibiotic.

    Product
    Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. Used in the semi-quantitative agar diffusion test method for in- vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-869-2014·2014-01-29

    Repaglinide Tablets Recalled Due to Potential Labeling Mixup

    Aidapak Services is recalling Repaglinide 2 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    REPAGLINIDE, Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00169008481.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-781-2014·2014-01-29

    Aidapak Recalls Tolterodine Tartrate ER Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Tolterodine Tartrate ER capsules because they may be mislabeled as other medications.

    Product
    TOLTERODINE TARTRATE ER, Capsule, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00009519101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0819-2014·2014-01-29

    FDA Recalls Composix L/P Mesh Due to Labeling Mismatch

    Davol, Inc. is recalling 19 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 10" X 13" Product Code 0144113 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-785-2014·2014-01-29

    Aidapak Recalls Pancrelipase DR Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Pancrelipase DR capsules because they may be mislabeled as other prescription drugs. The affected repacked drugs were distributed in four western states.

    Product
    PANCRELIPASE DR, Capsule, 24000 /76000 /120000 USP units, Rx only, Distributed by: AidaPak Service, LLC, NDC 00032122401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1021-2014·2014-01-29

    Aidapak Recalls Ascorbic Acid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Ascorbic Acid chew tablets because they may have been mislabeled as Phenol lozenges.

    Product
    ASCORBIC ACID, CHEW Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904052660.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-881-2014·2014-01-29

    Cilostazol Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Cilostazol 100 mg tablets because they may have been mislabeled as Triamterene/Hydrochlorothiazide.

    Product
    CILOSTAZOL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185022360.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-941-2014·2014-01-29

    Aidapak Recalls Pyridoxine HCL Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 50 mg Pyridoxine HCL tablets because they may have been mislabeled as other medications. The affected products were distributed in four western states.

    Product
    PYRIDOXINE HCL, Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536440801.
    Category
    Drug
    Distribution
    4 states