Trimix T 101 Alprostadil/Papverine/Phentolamine 5.9 mcg/17.65 mg/0.59 mcg per mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1336-05
Reported: November 7, 2018 Initiated: September 10, 2018 #D-0195-2019
Product Description
Trimix T 101 Alprostadil/Papverine/Phentolamine 5.9 mcg/17.65 mg/0.59 mcg per mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1336-05
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Pharm D Solutions, LLC
- Units Affected
- 20 milliliters
- Distribution
- Nationwide
- Location
- Houston, TX
Frequently Asked Questions
What product was recalled? ▼
Trimix T 101 Alprostadil/Papverine/Phentolamine 5.9 mcg/17.65 mg/0.59 mcg per mL Injectable, Pharm D Solutions, Houston, Texas --- NDC 69699-1336-05. Recalled by Pharm D Solutions, LLC. Units affected: 20 milliliters.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 7, 2018. Severity: Moderate. Recall number: D-0195-2019.
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