Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter
Pharmedium Services is recalling specific lots of Phenylephrine HCl injection due to the presence of human hair particulate matter.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of at least 4 per the rubric.
Plain-English summary
Pharmedium Services, LLC is recalling 24 bags of Phenylephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection USP. The product is packaged in 250 ml bags and is prescription only. The affected lots are 14309095S (Exp 02/03/15) and 14311008S (Exp 02/05/15).
The recall was initiated because the firm manufactured these products using Hospira 0.9% Sodium Chloride, USP injection, which was subsequently recalled due to the presence of particulate matter, specifically human hair. The distribution of the affected product was nationwide.
Healthcare providers and patients should check their inventory for the specific lot numbers and expiration dates listed above. If the product is found, it should be quarantined and not administered. Consumers should contact their healthcare provider or pharmacist for further instructions regarding the disposal or replacement of the medication.
The recalled product
- Product
- PHENYLephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection USP (160 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-169-50
- Manufacturer
- Pharmedium Services, LLC
- Category
- Drug — Injection
- Affected units
- 24
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (4)
- Lot #: 14309095S
- Exp 02/03/15
- 14311008S
- Exp 02/05/15
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 8 recalled by Pharmedium Services, LLC under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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