Drugs & medicalClass II

Denver Solutions, LLC DBA Leiters Health recalls Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796…

Labeling: Label Mix-up: Vials labeled as moxifloxacin 1 mg/mL may actually contain moxifloxacin 5 mg/mL

Read the official notice →
Date
2021-12-29
Country
United States
Brand
Denver Solutions, LLC DBA Leiters Health
Product
Moxifloxacin, 1 mg/mL, 1mL in 2mL vial, solution for intracameral injection, 10 vials/carton, Rx only, Leiters 13796 Compark Blvd,…
Classification
Class II
Units
Nationwide within the United States
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Denver Solutions, LLC DBA Leiters Health recalls

  1. 2025-04-30
  2. US
    Drugs & medicalClass II

    Denver Solutions, LLC DBA Leiters Health recalls Rocuronium Bromide 50 mg per 5mL (10mg per mL), 5mL Single Dose Syringe, Rx only, Leiters Health, 13796 Compark Blvd,…

    Lack of Assurance of Sterility: Leaking/damaged syringes.

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthNationwide in the U.S.AOfficial notice →
  3. 2024-03-06
  4. US
    Drugs & medicalClass II

    Denver Solutions, LLC DBA Leiters Health recalls Moxifloxacin 5mg/ml, 1 ml in a Single- Dose Vial, Rx Only, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC…

    Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthNationwide in the USAOfficial notice →
  5. 2024-02-07
  6. US
    Drugs & medicalClass I

    Denver Solutions, LLC DBA Leiters Health recalls VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark…

    Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthNationwide within the United StatesOfficial notice →
  7. 2023-11-01
  8. US
    Drugs & medicalClass III

    Denver Solutions, LLC DBA Leiters Health recalls VANCOmycin HCI PF, 1.25 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796…

    Labeling: Not Elsewhere Classified

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthUSA NationwideOfficial notice →
  9. 2023-03-15
  10. US
    Drugs & medicalClass II

    Denver Solutions, LLC DBA Leiters Health recalls Phenylephrine HCl 40 mg (160 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV Bag, Leiter Compounding Health 13796…

    CGMP DEVIATIONS

    FDA · DrugDenver Solutions, LLC DBA Leiters HealthNationwide within the United States including VA or other Government facilitiesOfficial notice →
All 6 Denver Solutions, LLC DBA Leiters Health recalls →

Other drugs & medical recalls in the United States

  1. 2021-12-29
  2. US
  3. US
    Drugs & medicalClass II

    Efficient Laboratories, Inc. recalls Rompe Pecho Max Multi-Symptoms Maximum Strength, 8 Fl. Oz. (237 mL) bottles, Distributed by: Efficient Laboratories, Inc. Miami, FL…

    Microbial Contamination of Non-Sterile Products

    FDA · DrugEfficient Laboratories, Inc.Nationwide within the United StatesOfficial notice →
  4. US
  5. US
    Drugs & medicalClass II

    Medline Industries Inc recalls Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and…

    Defective Container: Customer complaints for leaking bottles and dispensing issues.

    FDA · DrugMedline Industries IncNationwide in the USA, Canada, Hong Kong, and PeruOfficial notice →
  6. 2021-12-22
  7. US
    Drugs & medicalClass II

    Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls Medical Device Identification Cards associated with Sprint Quattro Lead, Product/CFN 6935M72

    The back of some Medical Device Identification Cards provided to patients were printed with an erroneous statement stating the following: "This patient has a complete MR conditional system implanted."

    FDA · DeviceMedtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)US, Canada, Northern Mariana IslandsOfficial notice →
  8. US
    Drugs & medicalClass II

    Xstrahl Limited recalls Treatment applicator for Gulmay Medical 150 or Xstrahl 150 superficial X-ray therapy system

    Base plate may detach from the main body of the treatment applicator.

    FDA · DeviceXstrahl LimitedUS and ALGERIA, AUSTRALIA, AUSTRIA, BULGARIA, CANADA, COSTA RICA, CROATIA,…Official notice →
See all drugs & medical recalls →