Demerol recall: Labeling Error
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.
Why was Demerol recalled?
Labeling; Missing label; ampoules are missing the immediate container label
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot: 221303A, 1OCT2014
- Product
- 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.
- Recalling firm
- Hospira Inc.
- Quantity
- 237,850 ampoules
- Distribution
- Nationwide
- Recall date
- April 16, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)