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Terminated

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.

FDA Recall Z-0044-2007 · Posted 2006-10-19

Recalling FirmExcelsior Medical Corp
Recall StatusTerminated
Product CodeNGT
Date Initiated2006-04-24
Date Terminated2006-10-26
Product Quantity466,000 units

Reason for Recall

The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.

Firm Action

Excelsior notified Hospira of the recall on 4/24/2006. Hospira notified Morris Dickson and Cardinal Health on 4/28/2006.

Root Cause

Other

Distribution Pattern

Worldwide.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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