Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Reported: June 19, 2019 Initiated: May 28, 2019 #D-1399-2019
Product Description
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.
Reason for Recall
Lack of Processing Controls.
Details
- Recalling Firm
- Synthetopes Inc
- Units Affected
- 20 vials
- Distribution
- Nationwide.
- Location
- Conway, SC
Frequently Asked Questions
What product was recalled? ▼
Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.. Recalled by Synthetopes Inc. Units affected: 20 vials.
Why was this product recalled? ▼
Lack of Processing Controls.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 19, 2019. Severity: Moderate. Recall number: D-1399-2019.
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