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Class II: temporary or reversible health riskOngoing

Denver Solutions, LLC DBA Leiters Health Moxifloxacin PF Recall

Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Int…

Denver Solutions, LLC DBA Leiters Health · Englewood, CO

Risk level
Class II
Reported by FDA
Mar 6, 2024
Recall ID
D-0361-2024
Check your lot numberHow we source this data

Summary

Denver Solutions, LLC DBA Leiters Health recalled Moxifloxacin PF starting Feb 20, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0361-2024 on Mar 6, 2024. Reason: Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination. Status: Ongoing.

Why it was recalled

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

Product description

Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42

Lot numbers, UPCs & expiration codes

Lot #:2331147, Exp:6-Mar-24; 2331180, Exp: 21-Mar-24; 2331256, Exp: 2-Apr-24; 2331279, Exp: 3-Apr-24; 2331283, Exp: 7-Apr-24; 2331345, Exp: 20-Apr-24; 2331422, Exp: 27-Apr-24; 2331563, Exp: 29-May-24.

Where it was sold

Nationwide in the USA

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0361-2024
Classification
Class II
Status
Ongoing
Recall initiated
Feb 20, 2024
FDA report date
Mar 6, 2024
Quantity
40,090 vials
Recall type
Voluntary: Firm initiated
Recalling firm
Denver Solutions, LLC DBA Leiters Health

Original FDA data

Every field from FDA enforcement report D-0361-2024, exactly as published.

Show all FDA fields
City
Englewood
State
CO
Status
Ongoing
Country
United States
Event ID
94071
Address
13796 Compark Blvd
Code information
Lot #:2331147, Exp:6-Mar-24; 2331180, Exp: 21-Mar-24; 2331256, Exp: 2-Apr-24; 2331279, Exp: 3-Apr-24; 2331283, Exp: 7-Apr-24; 2331345, Exp: 20-Apr-24; 2331422, Exp: 27-Apr-24; 2331563, Exp: 29-May-24.
Postal code
80112-7145
Report date
Mar 6, 2024
Product type
Drugs
Recall number
D-0361-2024
Classification
Class II
Recalling firm
Denver Solutions, LLC DBA Leiters Health
Product quantity
40,090 vials
Reason for recall
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt Solution (BSS) Sterile injection, Intracameral Use Only, Single- Dose Vial, Leiters 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-096-42
Distribution pattern
Nationwide in the USA
Recall initiation date
Feb 20, 2024
Initial firm notification
Letter
Center classification date
Feb 29, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0361-2024, published Mar 6, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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