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Class II: temporary or reversible health riskTerminated

Denver Solutions, LLC DBA Leiters Health Phenylephrine HCl 1mg per 10mL Recall

Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes, Rx only, Leiters 13796 Com…

Denver Solutions, LLC DBA Leiters Health · Englewood, CO

Risk level
Class II
Reported by FDA
Mar 15, 2023
Recall ID
D-0443-2023
Check your lot numberHow we source this data

Summary

Denver Solutions, LLC DBA Leiters Health recalled Phenylephrine HCl 1mg per 10mL starting Feb 21, 2023. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0443-2023 on Mar 15, 2023. Reason: CGMP DEVIATIONS. Status: Terminated.

Why it was recalled

CGMP DEVIATIONS

Product description

Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes, Rx only, Leiters 13796 Compark Blvd Englewood CO 80112, NDC 71449-001-15

Lot numbers, UPCs & expiration codes

Lot #: 2230895, Exp. Date 3/5/2023; 2230911, Exp. Date 3/11/2023; 2230913, Exp. Date 3/18/2023; 2230994, Exp. Date 3/27/2023; 2231006, Exp. Date 4/1/2023; 2231109, Exp. Date 4/19/2023; 2231126, Exp. Date 5/6/2023; 2231134, Exp. Date 5/10/2023; 2231140, Exp. Date 5/14/2023; 2231142, Exp. Date 5/20/2023; 2231156, Exp. Date 5/29/2023; 2231273, Exp. Date 6/3/2023; 2231285, Exp. Date 6/10/2023; 2231299, Exp. Date 6/17/2023; 2231331, Exp. Date 6/26/2023; 2330014, Exp. Date 7/9/2023; 2330025, Exp. Date 7/15/2023

Where it was sold

Nationwide within the United States including VA or other Government facilities

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-0443-2023
Classification
Class II
Status
Terminated
Recall initiated
Feb 21, 2023
FDA report date
Mar 15, 2023
Quantity
325,300 units
Recall type
Voluntary: Firm initiated
Recalling firm
Denver Solutions, LLC DBA Leiters Health

Original FDA data

Every field from FDA enforcement report D-0443-2023, exactly as published.

Show all FDA fields
City
Englewood
State
CO
Status
Terminated
Country
United States
Event ID
91762
Address
13796 Compark Blvd
Code information
Lot #: 2230895, Exp. Date 3/5/2023; 2230911, Exp. Date 3/11/2023; 2230913, Exp. Date 3/18/2023; 2230994, Exp. Date 3/27/2023; 2231006, Exp. Date 4/1/2023; 2231109, Exp. Date 4/19/2023; 2231126, Exp. Date 5/6/2023; 2231134, Exp. Date 5/10/2023; 2231140, Exp. Date 5/14/2023; 2231142, Exp. Date 5/20/2023; 2231156, Exp. Date 5/29/2023; 2231273, Exp. Date 6/3/2023; 2231285, Exp. Date 6/10/2023; 2231299, Exp. Date 6/17/2023; 2231331, Exp. Date 6/26/2023; 2330014, Exp. Date 7/9/2023; 2330025, Exp. Date 7/15/2023
Postal code
80112-7145
Report date
Mar 15, 2023
Product type
Drugs
Recall number
D-0443-2023
Classification
Class II
Recalling firm
Denver Solutions, LLC DBA Leiters Health
Product quantity
325,300 units
Termination date
Jan 11, 2024
Reason for recall
CGMP DEVIATIONS
Voluntary / mandated
Voluntary: Firm initiated
Product description
Phenylephrine HCl 1mg per 10mL (100 mcg/mL) 10 mL syringes, Rx only, Leiters 13796 Compark Blvd Englewood CO 80112, NDC 71449-001-15
Distribution pattern
Nationwide within the United States including VA or other Government facilities
Recall initiation date
Feb 21, 2023
Initial firm notification
E-Mail
Center classification date
Mar 7, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0443-2023, published Mar 15, 2023. View the source record (openFDA) · FDA enforcement reports

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

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