0.9% Sodium Chloride Flush Syringe, 2.5 mL. Product Code: E0100-30. Manufactured by Excelsior Medical and distributed by
FDA device recall Z-0044-2007 · posted 2006-10-19 · Terminated
Recall details
- Recalling firm
- Excelsior Medical Corp
- Reason for recall
- The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.
- Action taken
- Excelsior notified Hospira of the recall on 4/24/2006. Hospira notified Morris Dickson and Cardinal Health on 4/28/2006.
- Root cause
- Other
- Status
- Terminated
- Product code
- NGT
- Quantity affected
- 466,000 units
- Distribution
- Worldwide.
- Date initiated
- 2006-04-24
- Date posted
- 2006-10-19
- Date terminated
- 2006-10-26
- Location
- Neptune, NJ
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