The Recall Desk

Archive

January 2014 recalls

1,423 recalls were announced in January 2014.

What the numbers show

Critical
159
Severe
434
High
277
Moderate
532
Low
21

Of the 1,423 recalls this month scored against our rubric, 11% are Critical, 30% are Severe.

201–300 of 1423

  • ModerateFDA (Drugs)·D-914-2014·2014-01-29

    Aidapak Recalls Thyroid Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 60 mg Thyroid tablets that may have been mislabeled as 30 mg tablets.

    Product
    THYROID, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00456045901.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-907-2014·2014-01-29

    Aidapak Recalls Albuterol Sulfate ER Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Albuterol Sulfate ER 4 mg tablets that may have been mislabeled as Simvastatin 20 mg.

    Product
    ALBUTEROL SULFATE ER, Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378412201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-810-2014·2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Labeling Error

    Aidapak Services, LLC is recalling Levothyroxine Sodium tablets due to a potential label mixup with Magnesium Chloride. The repacked drugs were distributed in four western states.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 125 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00074706890.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-823-2014·2014-01-29

    Carbidopa/Levodopa Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Carbidopa/Levodopa tablets that may have been mislabeled as Digoxin. Patients should verify their medication labels.

    Product
    CARBIDOPA/LEVODOPA, Tablet, 25 mg/250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093029401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-845-2014·2014-01-29

    Aidapak Recalls Losartan Potassium Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Midodrine HCL 2.5 mg.

    Product
    LOSARTAN POTASSIUM, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093736598.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0792-2014·2014-01-29

    Remel Recalls Oxoid Cefpodoxime Antimicrobial Susceptibility Test Discs

    Remel Inc is recalling Oxoid Cefpodoxime 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.

    Product
    Oxoid Antimicrobial Susceptibility Test Discs, Cefpodoxime 10 mcg., CT1612B, 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-933-2014·2014-01-29

    Aidapak Recalls Cyanocobalamin Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 923 tablets of Cyanocobalamin 1000 mcg because they may have been mislabeled as other medications.

    Product
    CYANOCOBALAMIN, Tablet, 1000 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536355601.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-925-2014·2014-01-29

    Nicotine Polacrilex Gum Recalled for Potential Labeling Mixup

    Aidapak Services, LLC is recalling 2 mg Nicotine Polacrilex Gum due to a potential labeling mixup with Folic Acid or Quetiapine Fumarate tablets.

    Product
    NICOTINE POLACRILEX, GUM, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00536302923.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-878-2014·2014-01-29

    Fosinopril Sodium Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Mercaptopurine 50 mg.

    Product
    FOSINOPRIL SODIUM, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00185004109.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1005-2014·2014-01-29

    Mycophenolate Mofetil Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Mycophenolate Mofetil capsules because they may have been mislabeled as Atorvastatin or Propranolol.

    Product
    MYCOPHENOLATE MOFETIL, Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781206701.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1012-2014·2014-01-29

    Losartan Potassium Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Atorvastatin Calcium 80 mg.

    Product
    LOSARTAN POTASSIUM, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781570192.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0820-2014·2014-01-29

    FDA Recalls Composix L/P Mesh Due to Labeling Mismatch

    Davol, Inc. is recalling 46 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 6" X 8" Product Code 0144680 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 reconstruction…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-896-2014·2014-01-29

    Aidapak Recalls Mislabeled Triamterene/HCTZ Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling Triamterene/HCTZ tablets that may have been mislabeled as Caffeine tablets. The error involves a label mixup during repacking.

    Product
    TRIAMTERENE/HCTZ, Tablet, 37.5 mg/25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378135201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-962-2014·2014-01-29

    Verapamil Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Verapamil HCL tablets because they may have been mislabeled as Atorvastatin or Tacrolimus.

    Product
    VERAPAMIL HCL, Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591040401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-829-2014·2014-01-29

    Aidapak Recalls Nortriptyline Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Nortriptyline HCL capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.

    Product
    NORTRIPTYLINE HCL, Capsule, 75 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093081301.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-863-2014·2014-01-29

    Aidapak Recalls CapsuleTOPRIL Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling CapsuleTOPRIL tablets because they may have been mislabeled as Calcitriol capsules. The error could lead to patients receiving the wrong medication.

    Product
    CapsuleTOPRIL, Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00143117101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0795-2014·2014-01-29

    Remel Recalls Oxoid Ertapenem Antimicrobial Susceptibility Test Discs

    Remel Inc is recalling Oxoid Ertapenem 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.

    Product
    Oxoid Antimicrobial Susceptibility Test Discs, Ertapenem 10 mcg., CT1761B, 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-956-2014·2014-01-29

    Aidapak Recalls Liothyronine Sodium Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling 5 mcg Liothyronine Sodium tablets because they may have been mislabeled as 25 mcg tablets.

    Product
    LIOTHYRONINE SODIUM, Tablet, 5 mcg, NDC 00574022001, Rx only, Distributed by: AidaPak Service, LLC, NDC 00574022001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-782-2014·2014-01-29

    Aidapak Recalls Dronedarone HCL Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Dronedarone HCL 400 mg tablets because they may be mislabeled as Methylergonovine Maleate 0.2 mg.

    Product
    DRONEDARONE HCL, Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00024414260.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-868-2014·2014-01-29

    Aidapak Recalls Repaglinide Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Repaglinide 1 mg tablets because they may have been mislabeled as Valsartan, Guaifenesin, or Magnesium Chloride.

    Product
    REPAGLINIDE, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00169008281.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-885-2014·2014-01-29

    Aidapak Recalls Propranolol HCL ER Capsules Due to Labeling Error

    Aidapak Services, LLC is recalling Propranolol HCL ER capsules because they may have been mislabeled as Cinacalcet HCL tablets.

    Product
    PROPRANOLOL HCL ER, Capsule, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228277811.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-988-2014·2014-01-29

    Aidapak Recalls Oxybutynin Chloride Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling Oxybutynin Chloride 5 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    OXYBUTYNIN CHLORIDE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603497521.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-840-2014·2014-01-29

    FDA Recalls Nefazodone Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Nefazodone HCL 150 mg tablets because they may have been mislabeled as Liothyronine Sodium 25 mcg.

    Product
    NEFAZODONE HCL, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093711306.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-886-2014·2014-01-29

    Aidapak Recalls Hydrochlorothiazide Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Hydrochlorothiazide 12.5 mg tablets because they may have been mislabeled as other prescription drugs.

    Product
    HYDROCHLOROTHIAZIDE, Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228282011.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0817-2014·2014-01-29

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products COCM Reagent

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products COCM Reagent because of inaccurate quality control results. The recall affects 3,342 units distributed worldwide.

    Product
    VITROS Chemistry Products COCM Reagent
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-894-2014·2014-01-29

    Thiothixene Capsules Recalled for Potential Labeling Error

    Aidapak Services is recalling Thiothixene 1 mg capsules because they may have been mislabeled as Omega-3 Fatty Acid 1000 mg capsules.

    Product
    THIOTHIXENE, Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378100101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-871-2014·2014-01-29

    Fluconazole Tablets Recalled Due to Potential Labeling Errors

    Aidapak Services is recalling Fluconazole 200 mg tablets because they may have been mislabeled as Valsartan or Fluconazole 100 mg.

    Product
    FLUCONAZOLE, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00172541360.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-926-2014·2014-01-29

    Aidapak Recalls Acetaminophen Chew Tablets Due to Labeling Mixup

    Aidapak Services, LLC is recalling Acetaminophen chew tablets because they may have been mislabeled as other medications. The repacked drugs were distributed in four western states.

    Product
    ACETAMINOPHEN, CHEW Tablet, 80 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536323307.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-835-2014·2014-01-29

    Aidapak Recalls Pioglitazone Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Pioglitazone HCL 15 mg tablets because they may have been mislabeled as Doxycycline or Lovastatin.

    Product
    PIOGLITAZONE HCL, Tablet, 15 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093204856.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-793-2014·2014-01-29

    Aidapak Recalls Exemestane Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Exemestane 25 mg tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.

    Product
    EXEMESTANE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00054008013.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-789-2014·2014-01-29

    Lithium Carbonate ER Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Lithium Carbonate ER tablets due to a labeling error where they may be mislabeled as other medications.

    Product
    LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00054002025.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-939-2014·2014-01-29

    FDA Recalls Calcium Polycarbophil Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Calcium Polycarbophil tablets that may be mislabeled as Caffeine tablets. The error involves a label mixup during repacking.

    Product
    CALCIUM POLYCARBOPHIL, Tablet, 625 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536430611.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-852-2014·2014-01-29

    FDA Recalls Doxazosin Mesylate Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Doxazosin Mesylate 1 mg tablets that may be mislabeled as Pyridoxine HCl 100 mg.

    Product
    DOXAZOSIN MESYLATE, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00093812001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-936-2014·2014-01-29

    Aidapak Recalls Docusate Sodium Capsules Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 16,044 Docusate Sodium capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.

    Product
    DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536375710.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-864-2014·2014-01-29

    Aidapak Recalls CapsuleTOPRIL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling CapsuleTOPRIL 6.25 mg tablets because they may have been mislabeled as Lubiprostone 24 mcg capsules.

    Product
    CapsuleTOPRIL, Tablet, 6.25 mg (1/2 of 12.5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 00143117101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-749-2014·2014-01-29

    Novartis Recalls Theraflu Cold and Cough Powder Packets

    Novartis is recalling Theraflu Daytime Severe Cold & Cough powder packets and NeoCitran products due to the potential presence of foreign substances.

    Product
    Theraflu Daytime Severe Cold & Cough (acetaminophen 650 mg, dextromethorphan hydrobromide 20 mg, phenylephrine hydrochloride 10 mg) powder packets, Berry Infused with Menthol & Green Tea flavors, 6-count packets per carton, , Distributed by: Novartis Consumer Health, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-757-2014·2014-01-29

    Novartis Recalls NeoCitran Extra Strength Powder Packets Due to Foreign Substances

    Novartis Consumer Health is recalling NeoCitran Extra Strength powder packets because they may contain foreign substances. The products were distributed nationwide and internationally.

    Product
    NeoCitran Extra Strength (acetaminophen 650 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 20mg, chlorpheniramine maleate 4 mg, ascorbic acid 5 mg) powder packets, Soothing Lemon flavor, 10-single dose pouches per carton, Novartis Consumer Health Canada…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-945-2014·2014-01-29

    Aidapak Recalls Niacin TR Tablets Due to Potential Label Mixup

    Aidapak Services is recalling Niacin TR 1000 mg tablets because they may have been mislabeled as 750 mg tablets. The repacked drugs were distributed in four western states.

    Product
    NIACIN TR, Tablet, 1000 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00536703801.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1004-2014·2014-01-29

    Terazosin HCL Capsules Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Terazosin HCL 5 mg capsules due to a potential label mixup with Doxazosin Mesylate 1 mg tablets.

    Product
    TERAZOSIN HCL, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781205301.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-884-2014·2014-01-29

    Aidapak Recalls Gabapentin Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Gabapentin 600 mg tablets because they may have been mislabeled as Aripiprazole 15 mg.

    Product
    GABAPENTIN, Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00228263611.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-753-2014·2014-01-29

    Novartis Recalls Theraflu MAX-D Powder Packets Due to Foreign Substances

    Novartis Consumer Health is recalling Theraflu MAX-D and NeoCitran powder packets because they may contain foreign substances.

    Product
    Theraflu MAX-D Severe Cold & Flu (acetaminophen 1000 mg, dextromethorphan HBr 30 mg, guaifenesin 400 mg, pseudoephedrine HCl 60 mg) powder packets, Natural Citrus flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-984-2014·2014-01-29

    Aidapak Recalls Hydrocortisone Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling 5 mg hydrocortisone tablets because they may have been mislabeled as other prescription drugs.

    Product
    HYDROCORTISONE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603389919.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0815-2014·2014-01-29

    Bard Access Systems Recalls Low Profile Ports with Undersized Catheters

    Bard Access Systems is recalling Low Profile Ports with 6.6 Fr catheters because some silicone catheters may be undersized to 5.3 Fr.

    Product
    Titanium Single Lumen Low-Profile port, with Pre-Attached open-Ended Silicone 6.6Fr Catheter. Product Code 0602180 Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-918-2014·2014-01-29

    Sodium Chloride Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling 1,000 mg sodium chloride tablets that may be mislabeled as repaglinide. The error involves specific lots distributed in four western states.

    Product
    SODIUM CHLORIDE, Tablet, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00527111610
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-910-2014·2014-01-29

    Fluvastatin Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Fluvastatin 20 mg capsules because they may have been mislabeled as a different medication.

    Product
    FLUVASTATIN, Capsule, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378802077.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1000-2014·2014-01-29

    Aidapak Recalls Isosorbide Dinitrate Tablets Due to Labeling Errors

    Aidapak Services, LLC is recalling Isosorbide Dinitrate 10 mg tablets because they may have been mislabeled as Sodium Chloride or Calcitriol.

    Product
    ISOSORBIDE DINITRATE, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781155601.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-888-2014·2014-01-29

    Metoprolol Tartrate Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Metoprolol Tartrate 25 mg tablets because they may have been mislabeled as Docusate Sodium 250 mg capsules.

    Product
    METOPROLOL TARTRATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378001801.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-891-2014·2014-01-29

    Aidapak Recalls Atropine Sulfate/Diphenoxylate Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling Atropine Sulfate/Diphenoxylate HCL tablets because they may have been mislabeled as Cyanocobalamin or Tri-Buffered Aspirin.

    Product
    ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378041501.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-930-2014·2014-01-29

    Aidapak Recalls Multivitamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling specific lots of multivitamin chew tablets because they may have been mislabeled as other drugs.

    Product
    MULTIVITAMIN/MULTIMINERAL, CHEW Tablet, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536344308.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1028-2014·2014-01-29

    Aidapak Recalls Niacin Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Niacin 500 mg tablets because they may have been mislabeled as Naproxen or Docusate Sodium.

    Product
    NIACIN, Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904227260.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-821-2014·2014-01-29

    Desloratadine Tablets Recalled for Potential Labeling Mixup

    Aidapak Services, LLC is recalling Desloratadine 5 mg tablets due to a potential label mixup with Ascorbic Acid 250 mg tablets.

    Product
    DESLORATADINE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00085126401.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1013-2014·2014-01-29

    Aidapak Recalls Amantadine HCL Tablets Due to Labeling Error

    Aidapak Services, LLC is recalling Amantadine HCL 100 mg tablets because they may have been mislabeled as other medications.

    Product
    AMANTADINE HCL, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00832011100.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-931-2014·2014-01-29

    Aidapak Recalls Cyanocobalamin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 100 mcg cyanocobalamin tablets because they may have been mislabeled as guaiFENesin ER 600 mg tablets.

    Product
    CYANOCOBALAMIN, Tablet, 100 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536354201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-916-2014·2014-01-29

    Potassium Acid Phosphate Tablets Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Potassium Acid Phosphate tablets due to a potential label mixup with prednisone. The repacked drugs were distributed in four western states.

    Product
    POTASSIUM ACID PHOSPHATE, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00486111101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-943-2014·2014-01-29

    FDA Recalls Vitamin B Complex Capsules Due to Labeling Error

    Aidapak Services is recalling Vitamin B Complex capsules that may have been mislabeled as Acarbose tablets. The error involves a label mixup.

    Product
    VITAMIN B COMPLEX, Capsule, 0 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00536478701.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-780-2014·2014-01-29

    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 Ranolazine ER or Ferrous Sulfate.

    Product
    TOLTERODINE TARTRATE ER, Capsule, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00009519001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-833-2014·2014-01-29

    Aidapak Recalls Sotalol HCL Tablets Due to Potential Labeling Errors

    Aidapak Services, LLC is recalling Sotalol HCL 80 mg tablets because they may have been mislabeled as Diltiazem HCL or Propranolol HCL ER.

    Product
    SOTALOL HCL, Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093106101.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-778-2014·2014-01-29

    Aidapak Recalls Mislabeled Pantoprazole Sodium DR Tablets

    Aidapak Services is recalling 20 mg Pantoprazole Sodium DR tablets because they may be mislabeled as Hyoscyamine Sulfate or Multivitamin/Multimineral.

    Product
    PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00008060601.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0814-2014·2014-01-29

    Bard Access Systems Recalls MRI Low Profile Ports with Undersized Catheters

    Bard Access Systems is recalling MRI Low Profile Single Lumen ports because some silicone catheters may be undersized to 5.3 Fr instead of the labeled 6.6 Fr.

    Product
    MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Catheter. Product Code 0603880. Product Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in BardPort…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-769-2014·2014-01-29

    Raloxifene HCL Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Raloxifene HCL tablets due to a potential label mixup with Isosorbide Mononitrate.

    Product
    RALOXIFENE HCL, Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00002416530.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-807-2014·2014-01-29

    Aidapak Recalls Phenytoin Sodium ER Capsules Due to Labeling Error

    Aidapak Services is recalling Phenytoin Sodium ER capsules because they may have been mislabeled as Lithium Carbonate ER tablets.

    Product
    PHENYTOIN SODIUM ER, Capsule, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00071374066.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1015-2014·2014-01-29

    FDA Recalls Chlorpromazine Tablets Due to Potential Labeling Mixup

    Aidapak Services is recalling chlorpromazine HCl tablets that may be mislabeled as acyclovir or trimethobenzamide. The error occurred during repacking in four western states.

    Product
    chlorproMAZINE HCl, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00832030300.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-905-2014·2014-01-29

    Temazepam Capsules Recalled for Potential Labeling Mixup

    Aidapak Services is recalling Temazepam 7.5 mg capsules because they may be mislabeled as Calcium Citrate or Valsartan.

    Product
    TEMAZEPAM, Capsule, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378311001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-843-2014·2014-01-29

    Aidapak Recalls Mislabeled Amlodipine Tablets Due to Label Mixup

    Aidapak Services, LLC is recalling 5 mg amlodipine besylate tablets that may have been mislabeled as cyanocobalamin. The error involves a label mixup affecting specific lots.

    Product
    amLODIPine BESYLATE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093716798.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-997-2014·2014-01-29

    FDA Recalls Trifluoperazine Tablets Due to Potential Labeling Error

    Aidapak Services is recalling Trifluoperazine HCL tablets because they may have been mislabeled as Terbutaline Sulfate.

    Product
    TRIFLUOPERAZINE HCL, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781103001.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-1023-2014·2014-01-29

    Aidapak Recalls Niacin TR Capsules Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Niacin TR capsules because they may have been mislabeled as Methylergonovine Maleate tablets.

    Product
    NIACIN TR, Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904062960.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-967-2014·2014-01-29

    Aidapak Recalls Dicyclomine HCL Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling Dicyclomine HCL 20 mg tablets because they may have been mislabeled as Ramipril 2.5 mg capsules.

    Product
    DICYCLOMINE HCL, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591079501.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0799-2014·2014-01-29

    Zeiss Compensator Slider Lambda 6x20 Recalled for Misalignment

    Carl Zeiss Microscopy is recalling the Compensator Slider Lambda 6x20 component due to misalignment of the lambda plate.

    Product
    Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-994-2014·2014-01-29

    Sulfasalazine Tablets Recalled for Potential Labeling Mixup

    Aidapak Services is recalling 500 mg sulfasalazine tablets that may be mislabeled as fluconazole or phenytoin sodium.

    Product
    sulfaSALAzine, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00603580121.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-874-2014·2014-01-29

    Omega-3 Acid Ethyl Esters Capsules Recalled for Potential Label Mixup

    Aidapak Services, LLC is recalling Omega-3 Acid Ethyl Esters capsules due to a potential label mixup with other medications. The repacked drugs were distributed in four western states.

    Product
    OMEGA-3-ACID ETHYL ESTERS, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00173078302.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-760-2014·2014-01-29

    Novartis Recalls NeoCitran DM Cough and Cold Powder Packets

    Novartis is recalling NeoCitran DM Cough & Cold powder packets because they may contain foreign substances. The products were distributed in the U.S., Canada, and other countries.

    Product
    NeoCitran DM Cough & Cold (dextromethorphan hydrobromide 30 mg, phenylephrine hydrochloride 10 mg, pheniramine maleate 20 mg) powder packets, Natural Source Lemon flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, UPC 0 58478…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-966-2014·2014-01-29

    FDA Recalls Propafenone HCL Tablets Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling Propafenone HCL 150 mg tablets because they may have been mislabeled as Fosinopril Sodium 10 mg tablets.

    Product
    PROPAFENONE HCL, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591058201.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-882-2014·2014-01-29

    Aidapak Recalls Candesartan Cilexetil Tablets Due to Potential Labeling Error

    Aidapak Services, LLC is recalling Candesartan Cilexetil 16 mg tablets because they may have been mislabeled as Irbesartan 150 mg.

    Product
    CANDESARTAN CILEXETIL, Tablet, 16 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00186001631.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-972-2014·2014-01-29

    Aidapak Recalls Cyclobenzaprine Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 5 mg cyclobenzaprine tablets because they may have been mislabeled as ascorbic acid or atenolol.

    Product
    CYCLOBENZAPRINE HCL, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00591325601.
    Category
    Drug
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-899-2014·2014-01-29

    Levothyroxine Sodium Tablets Recalled for Potential Label Mixup

    Aidapak Services is recalling Levothyroxine Sodium tablets that may have been mislabeled as Pramipexole Di-HCl.

    Product
    LEVOTHYROXINE SODIUM, Tablet, 175 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00378181701
    Category
    Drug
    Distribution
    4 states
  • 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

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