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Class II: temporary or reversible health riskOngoing

Denver Solutions, LLC DBA Leiters Health PHENYLephrine HCl in 0 Recall

PHENYLephrine HCl in 0

Denver Solutions, LLC DBA Leiters Health · Englewood, CO

Risk level
Class II
Reported by FDA
Apr 30, 2025
Recall ID
D-0372-2025
Check your lot numberHow we source this data

Summary

Denver Solutions, LLC DBA Leiters Health recalled PHENYLephrine HCl in 0 starting Mar 31, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0372-2025 on Apr 30, 2025. Reason: Lack of Assurance of Sterility: Leaking/damaged syringes. Status: Ongoing.

Why it was recalled

Lack of Assurance of Sterility: Leaking/damaged syringes.

Product description

PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,

Lot numbers, UPCs & expiration codes

Lot #: 2431349A, Exp.: 6/16/2025

Where it was sold

Nationwide in the U.S.A

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-0372-2025
Classification
Class II
Status
Ongoing
Recall initiated
Mar 31, 2025
FDA report date
Apr 30, 2025
Quantity
7,290 syringes
Recall type
Voluntary: Firm initiated
Recalling firm
Denver Solutions, LLC DBA Leiters Health

Original FDA data

Every field from FDA enforcement report D-0372-2025, exactly as published.

Show all FDA fields
City
Englewood
State
CO
Status
Ongoing
Country
United States
Event ID
96607
Address
13796 Compark Blvd
Code information
Lot #: 2431349A, Exp.: 6/16/2025
Postal code
80112-7145
Report date
Apr 30, 2025
Product type
Drugs
Recall number
D-0372-2025
Classification
Class II
Recalling firm
Denver Solutions, LLC DBA Leiters Health
Product quantity
7,290 syringes
Reason for recall
Lack of Assurance of Sterility: Leaking/damaged syringes.
Voluntary / mandated
Voluntary: Firm initiated
Product description
PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg per 5mL (100 mcg/mL), 5 mL Single Dose Syringe, Rx Only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112. NDC: 71449-001-11,
Distribution pattern
Nationwide in the U.S.A
Recall initiation date
Mar 31, 2025
Initial firm notification
Letter
Center classification date
Apr 18, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0372-2025, published Apr 30, 2025. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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