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Class I: serious health riskOngoing

Denver Solutions, LLC DBA Leiters Health VANCOmycin HCl PF 1 Recall

VANCOmycin HCl PF 1

Denver Solutions, LLC DBA Leiters Health · Englewood, CO

Risk level
Class I
Reported by FDA
Feb 7, 2024
Recall ID
D-0281-2024
Check your lot numberHow we source this data

Summary

Denver Solutions, LLC DBA Leiters Health recalled VANCOmycin HCl PF 1 starting Dec 28, 2023. The FDA classified it as Class I (serious health risk) and published enforcement report D-0281-2024 on Feb 7, 2024. Reason: Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags. Status: Ongoing.

Why it was recalled

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

Product description

VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-028-68.

Lot numbers, UPCs & expiration codes

Lot #: 2331184, Exp. Date 02/13/2024; 2331185, Exp. Date 02/10/2024; 2331189, Exp. Date 02/20/2024; 2331191, Exp. Date 02/24/2024; 2331258,Exp. Date 03/03/2024; 2331317, Exp. Date 03/15/2024.

Where it was sold

Nationwide within the United States

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-0281-2024
Classification
Class I
Status
Ongoing
Recall initiated
Dec 28, 2023
FDA report date
Feb 7, 2024
Quantity
10,152 IV bags
Recall type
Voluntary: Firm initiated
Recalling firm
Denver Solutions, LLC DBA Leiters Health

Original FDA data

Every field from FDA enforcement report D-0281-2024, exactly as published.

Show all FDA fields
City
Englewood
State
CO
Status
Ongoing
Country
United States
Event ID
93710
Address
13796 Compark Blvd
Code information
Lot #: 2331184, Exp. Date 02/13/2024; 2331185, Exp. Date 02/10/2024; 2331189, Exp. Date 02/20/2024; 2331191, Exp. Date 02/24/2024; 2331258,Exp. Date 03/03/2024; 2331317, Exp. Date 03/15/2024.
Postal code
80112-7145
Report date
Feb 7, 2024
Product type
Drugs
Recall number
D-0281-2024
Classification
Class I
Recalling firm
Denver Solutions, LLC DBA Leiters Health
Product quantity
10,152 IV bags
Reason for recall
Superpotent Drug: semi-automated IV bag filling system can malfunction and provide a double dose of drug product to IV bags.
Voluntary / mandated
Voluntary: Firm initiated
Product description
VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag, Item F3206, for IV use only; Leiters 13796 Compark Blvd Englewood, CO 80112; NDC 71449-028-68.
Distribution pattern
Nationwide within the United States
Recall initiation date
Dec 28, 2023
Initial firm notification
E-Mail
Center classification date
Jan 29, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0281-2024, published Feb 7, 2024. View the source record (openFDA) · FDA enforcement reports

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

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