Pentreotide recall
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Why was Pentreotide recalled?
Lack of Processing Controls.
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?
All lots remaining within expiry.
- Product
- Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
- Recalling firm
- Synthetopes Inc
- Quantity
- 20 vials
- Distribution
- Nationwide.
- Recall date
- June 19, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)