PHENYLephrine 50 mg in 0.9% Sodium Chloride recall: Sterility Concern
PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0820-40
Why was PHENYLephrine 50 mg in 0.9% Sodium Chloride recalled?
Lack of Assurance of Sterility; product has the potential to leak.
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?
Lots: 20170512@6 BUD: 8/10/2017; 20170511@56 BUD: 8/9/2017
- Product
- PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0820-40
- Recalling firm
- SCA Pharmaceuticals
- Quantity
- N/A
- Distribution
- Nationwide
- Recall date
- August 2, 2017
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)