Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.
Reported: April 16, 2014 Initiated: March 25, 2014 #D-1226-2014
Product Description
Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.
Reason for Recall
Labeling; Missing label; ampoules are missing the immediate container label
Details
- Recalling Firm
- Hospira Inc.
- Units Affected
- 237,850 ampoules
- Distribution
- Nationwide
- Location
- Lake Forest, IL
Frequently Asked Questions
What product was recalled? ▼
Demerol, meperidine HCL Inj. USP, 25 mg/0.5 mL (50 mg/mL), 0.5 mL ampoules, Rx only, NDC 0409-1203-01, Hospira, Inc., Lake Forest, IL.. Recalled by Hospira Inc.. Units affected: 237,850 ampoules.
Why was this product recalled? ▼
Labeling; Missing label; ampoules are missing the immediate container label
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 16, 2014. Severity: Low. Recall number: D-1226-2014.
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