Recall Z-2395-2012— Hospira Inc.
Class II · Terminated
Class II FDA medical device recall by Hospira Inc., initiated 2012-08-28, terminated 2013-09-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated containers are used for mixing compatible medications or blood collections.. Reason: Embedded iron oxide glass defect which may have the potential to break off into the solution..
- Recalling firm
- Hospira Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2012-08-28
- Terminated
- 2013-09-18
- Firm location
- Lake Forest, IL, United States
Product description
Empty Evacuated Container 250 mL and 1000 mL. Empty Evacuated containers are used for mixing compatible medications or blood collections.
Reason for recall
Embedded iron oxide glass defect which may have the potential to break off into the solution.
Data sourced from openFDA. This site is unofficial and independent of the FDA.