Heparin Syringe FDA Report
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
AM2 PAT, Inc. Issues Nationwide Recall of Pre-Filled Heparin Lock Flush Solution USP
(5 mL in 12 mL Syringes)
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Contact:
AM2PAT, INC.
919-552-9689
FOR IMMEDIATE RELEASE --ANGIER, NC -- December 20, 2007 --- AM2 PAT, Inc., Angier, North Carolina, is initiating a nationwide recall of one lot of Pre-Filled Heparin Lock Flush Solution USP (5 mL in 12 mL Syringes), Lot # 070926H. The heparin IV flush syringes have been found to be contaminated with Serratia marcescens, which have resulted in patient infections. CDC has confirmed growth of Serratia marcescens from several unopened syringes of this product.
This type of bacterial infection could present a serious adverse health consequence that could lead to life-threatening injuries and/or death.
Consumers and user facilities who have these recalled pre-filled syringes, Heparin Lock Flush Solution USP, should stop using the product immediately. Please quarantine the affected product in your inventory and return it to your distributor immediately.
The following information for this recall includes:
MANUFACTURER: Sierra Pre-Filled, Inc., Angier, North Carolina
PRODUCT DESCRIPTION: Heparin Lock Flush Solution USP, 100 units/ml, 5ml in pre-filled syringes.
LOT# 070926H
NDC# 64054-1003-02
CATALOG# 1003-02
The firm voluntarily recalled this product after confirming bacterial contamination in some end user samples.
This product was distributed nationwide including the following states: Florida, Texas, Illinois, Colorado, and Pennsylvania.
It appears from an ongoing Food and Drug Administration (FDA) inspection of AM2 PAT, Inc.’s facility that the firm is not in compliance with the Quality System regulation and failed to have adequate controls to ensure necessary sterility of its pre-filled syringes.
The firm is continuing to work with FDA and CDC on monitoring this situation and FDA will provide continuing updates.
Consumers with questions may contact the company at 1-919-552-9689 or 847-691-6500 { MONDAY THROUGH FRIDAY 9AM EASTERN TILL 5PM EASTERN }
Any adverse reactions experienced with the use of this product, and/or quality problems should also be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch.
Florida Heparin Syringe Recall
In Flordida, state health officials have contacted hospital infection control professionals, county health departments, and eight distributors who serve the state. The distributors of Heparin have voluntarily agreed to discontinue release of the drug and have contacted their clients who may have received tainted product. Individuals who may have used lot #070926H of the Sierra pre-filled Heparin flush should immediately stop using the flush and contact their healthcare provider for a replacement supply and seek immediate medical attention if they develop a fever or other signs of an infection.
Heparin Syringe Recall Lawsuit
If you or a loved one have suffered an injury and contracted the Serratia Marcescens bacteria after using Sierra Heparin Lock Flush Solution syringes, then you should contact us immediately to talk to a Board Certified Personal Injury Trial Lawyer, certified by the Texas Board of Legal Specialization. Nationwide Assistance is available and our consultation is free and confidential. Write us online or call us: Toll Free 1-800-883-9858.
 Click Here for a Free Lawsuit Case Evaluation |
