Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
Reported: November 7, 2018 Initiated: September 10, 2018 #D-0143-2019
Product Description
Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Pharm D Solutions, LLC
- Units Affected
- 115 milliliters
- Distribution
- Nationwide
- Location
- Houston, TX
Frequently Asked Questions
What product was recalled? ▼
Bi-Mix Injection (Alprostadil 80 mcg/Lidocaine 2 mg/mL) Pharm D Solutions, Houston, Texas --- NDC 69699-1317-03. Recalled by Pharm D Solutions, LLC. Units affected: 115 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-0143-2019.
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