Alprostadil 500 mcg/mL Injectable recall
Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
Why was Alprostadil 500 mcg/mL Injectable recalled?
Incorrect Product Formulation
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: 03192018@42 Discard after 9/15/2018
- Product
- Alprostadil 500 mcg/mL Injectable, Vials, Westlab Pharmacy, Inc., Gainesville, FL 32607 NDC 10002-7335-00
- Recalling firm
- Westlab Pharmacy, Inc. dba Westlab Pharmacy
- Quantity
- 80 syringes
- Distribution
- Nationwide
- Recall date
- October 31, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)