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U.S. Department of Health and Human Services

Medical Device Recalls
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  Medical Device Recalls see related information
Date Initiated by Firm April 24, 2006
Create Date October 19, 2006
Recall Status1 Terminated 3
Recall Number Z-0044-2007
Recall Event ID 35960
Product 0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex.
Code Information Product E0100-30, Lot 22-010-9D
Recalling Firm/
Manufacturer		 Excelsior Medical Corp
1923 Heck Ave
Neptune NJ 07753-4428
For Additional Information Contact Himanshu Naik
732-643-6080
Manufacturer Reason
for Recall		 The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.
Action Excelsior notified Hospira of the recall on 4/24/2006. Hospira notified Morris Dickson and Cardinal Health on 4/28/2006.
Quantity in Commerce 466,000 units
Distribution Worldwide.
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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