Phenylephrine in 0.9% Sodium Chloride Injection recall: Labeling Error
Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton…
Why was Phenylephrine in 0.9% Sodium Chloride Injection recalled?
Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
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 #: 240310003D, Exp 6/4/2024
- Product
- Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables USA Inc, 36 Stults Road, Dayton…
- Recalling firm
- Hikma Injectables USA Inc
- Distribution
- CO, GA, PA, SD, WA
- Recall date
- May 29, 2024
- Classification
- Class I
- Status
- Completed
- Agency
- FDA (drug)