Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05
Reported: September 23, 2015 Initiated: August 20, 2015 #D-0418-2015
Product Description
Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05
Reason for Recall
Defective Container: There were customer complaints of cracked and leaking glass vials.
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 83,320 vials
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05. Recalled by Hospira Inc.. Units affected: 83,320 vials.
Why was this product recalled? ▼
Defective Container: There were customer complaints of cracked and leaking glass vials.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on September 23, 2015. Severity: Moderate. Recall number: D-0418-2015.
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