phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Reported: January 8, 2025 Initiated: December 19, 2024 #D-0174-2025
Product Description
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25
Reason for Recall
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Details
- Recalling Firm
- Hikma Injectables USA Inc
- Distribution
- Nationwide in the USA
- Location
- Dayton, NJ
Frequently Asked Questions
What product was recalled? ▼
phenylephrine in 0.9% Sodium Chloride Inj, 1mg per 10 mL (100 mcg/mL), Rx only, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, NDC 63037-173-25. Recalled by Hikma Injectables USA Inc.
Why was this product recalled? ▼
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 8, 2025. Severity: Moderate. Recall number: D-0174-2025.
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