Class II
Terminated
Propofol Injectable Emulsion, 1%, 200 mg/20 mL, (10mg/mL), 20 mL, Single patient infusion vial, Contains Benzyl Alcohol, For I.V. Administration, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-4699-30
This recall has been terminated (originally issued February 4, 2015).
- Company
- Hospira Inc.
- Recall Initiated
- December 23, 2014
- Posted
- February 4, 2015
- Recall Number
- D-0381-2015
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 126,075 vials
- Firm Location
- Lake Forest, IL, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter: The firm received a complaint of an embedded particulate in the neck of one vial composed primarily of iron.
Distribution
Nationwide
Lot / Code Info
Lot 35-844-DJ, Exp 11/01/2015
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