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Class I: serious health riskTerminated

Pharmedium Services HEPARIN Sodium Injection Recall

HEPARIN Sodium Injection USP, 12,500 USP Units added to 250 mL 5% Dextrose Injection US…

Pharmedium Services, LLC · Lake Forest, IL

Risk level
Class I
Reported by FDA
Sep 2, 2015
Recall ID
D-1355-2015
Check your lot numberHow we source this data

Summary

Pharmedium Services recalled HEPARIN Sodium Injection starting Apr 13, 2015. The FDA classified it as Class I (serious health risk) and published enforcement report D-1355-2015 on Sep 2, 2015. Reason: Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were subsequently recalled by the manufacturer due to the presence of particulate matter. Status: Terminated.

Why it was recalled

Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were subsequently recalled by the manufacturer due to the presence of particulate matter.

Product description

HEPARIN Sodium Injection USP, 12,500 USP Units added to 250 mL 5% Dextrose Injection USP (50 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0418, NDC# 61553-418-02.

Lot numbers, UPCs & expiration codes

Lot #: 15041123S, 15041003S, Exp 04/16/15

Where it was sold

Nationwide

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-1355-2015
Classification
Class I
Status
Terminated
Recall initiated
Apr 13, 2015
FDA report date
Sep 2, 2015
Quantity
480 bags
Recall type
Voluntary: Firm initiated
Recalling firm
Pharmedium Services, LLC

Original FDA data

Every field from FDA enforcement report D-1355-2015, exactly as published.

Show all FDA fields
City
Lake Forest
State
IL
Status
Terminated
Country
United States
Event ID
71846
Address
150 N Field Dr Ste 350
Code information
Lot #: 15041123S, 15041003S, Exp 04/16/15
Postal code
60045-2506
Report date
Sep 2, 2015
Product type
Drugs
Recall number
D-1355-2015
Classification
Class I
Recalling firm
Pharmedium Services, LLC
Product quantity
480 bags
Termination date
Jan 23, 2017
Reason for recall
Presence of Particulate Matter: The firm produced products using 0.9% Sodium Chloride Injection, USP or 5% Dextrose Injection, USP which were subsequently recalled by the manufacturer due to the presence of particulate matter.
Voluntary / mandated
Voluntary: Firm initiated
Product description
HEPARIN Sodium Injection USP, 12,500 USP Units added to 250 mL 5% Dextrose Injection USP (50 units per mL), packaged in 250 mL bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd #130, Sugar Land, TX 77478, Service Code 2K0418, NDC# 61553-418-02.
Distribution pattern
Nationwide
Recall initiation date
Apr 13, 2015
Initial firm notification
E-Mail
Center classification date
Aug 25, 2015

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1355-2015, published Sep 2, 2015. View the source record (openFDA) · FDA enforcement reports

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

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