Drugs & medicalClass II

RemedyRepack Inc. recalls Losartan HCTZ 50/12.5 mg, 90 count bottle Original NDC# 33342-0050-10 Repackaged NDC# 70518-3231-00

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

Read the official notice →
Date
2022-06-01
Country
United States
Brand
RemedyRepack
Product
Losartan HCTZ 50/12.5 mg, 90 count bottle Original NDC# 33342-0050-10 Repackaged NDC# 70518-3231-00
Classification
Class II
Units
Recalled product was distributed to Florida.
Category
Drugs & medical
Source
FDA · Drug

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More RemedyRepack recalls

  1. 2022-12-14
  2. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ…

    Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.

    FDA · DrugRemedyRepack Inc.Product was distributed to two different customers in MI.Official notice →
  3. 2022-09-21
  4. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Lisinopril 10 mg tablets, 30-count Blister Card, Rx Only, MFG: Lupin Pharma, Baltimore, MD Repackaged by: RemedyRepack Inc, Indiana PA.…

    Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.

    FDA · DrugRemedyRepack Inc.Distributed to two direct accounts in PA and AK.Official notice →
  5. 2022-06-01
  6. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

    FDA · DrugRemedyRepack Inc.Product was distributed to FL, SC and VAOfficial notice →
  7. 2022-05-04
  8. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Losartan Potassium 50 mg Tablet, a) 30-count blister card (NDC# 70518-3282-1), b) 60-count blister card (NDC: 70518-3282-0), Rx Only, MFG…

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

    FDA · DrugRemedyRepack Inc.Product was distributed to customers in AK and PA.Official notice →
  9. 2022-01-19
  10. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Metformin 750 mg Extended Release NDC # 70518-2920-00

    CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.

    FDA · DrugRemedyRepack Inc.Product was distributed to one direct account in PA.Official notice →
  11. 2022-01-12
  12. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Cefixime 400 mg capsule, packaged in a) 2-count bottle (NDC 70518-2749-02), b) 2-count blister pack (NDC 70518-2749-03), Rx only, MFG:…

    Failed Impurities/Degradation Specifications

    FDA · DrugRemedyRepack Inc.Product was distributed to two direct accounts in MI and PA.Official notice →
All 17 RemedyRepack recalls →

Other drugs & medical recalls in the United States

  1. 2022-06-01
  2. US
    Drugs & medicalClass II

    Noven Pharmaceuticals Inc recalls Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours (1.1 mg/hr) Contains: 30 Patches, Rx only, Manufactured for…

    Defective Delivery System: customer complaints exceeded respective action limits.

    FDA · DrugNoven Pharmaceuticals IncNationwide to the U.S. MarketOfficial notice →
  3. US
    Drugs & medicalClass II

    Direct Rx recalls Zonisamide Capsules USP, 100 mg, 90-count bottle, Rx Only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, Manufactured for:…

    CGMP Deviations: Gaps in the quality system in the Quality Control microbiology laboratory.

    FDA · DrugDirect RxNationwide to the U.S. marketOfficial notice →
  4. US
    Drugs & medicalClass II

    RemedyRepack Inc. recalls Losartan HCTZ 100/25 mg, 90 count bottles NDC# 70518-2578-00 Repackaged NDC Original NDC # 68180-0217-09

    CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

    FDA · DrugRemedyRepack Inc.Product was distributed to FL, SC and VAOfficial notice →
  5. 2022-05-25
  6. US
    Drugs & medicalClass II

    Caire, Inc. recalls CAIRE FreeStyle Comfort Portable Oxygen Concentrator with autoSAT, UltraSense and autoDOSE, model #AS200-3

    The device was not cleared for U.S. distribution.

    FDA · DeviceCaire, Inc.Distribution was made to Puerto Rico. There was no foreign/government/military…Official notice →
  7. US
    Drugs & medicalClass II

    Olympus Corporation of the Americas recalls Olympus Uretero-reno videoscope, Model No. URF-V2

    The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.

    FDA · DeviceOlympus Corporation of the AmericasUS Nationwide distribution in the state of AZ.Official notice →
  8. US
    Drugs & medicalClass II

    Radiometer Medical ApS recalls Radiometer, REF:956-552, PIC050- Arterial Blood Sampler 1 X 2 mL, 80 IU electrolyte-balanced heparin. Not for injection. , IVD, Rx Only,…

    Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf life of the product.

    FDA · DeviceRadiometer Medical ApSWorldwide distribution - US Nationwide distribution in the states of AZ, CA,…Official notice →
See all drugs & medical recalls →