Fentanyl 1,500 mcg/30 mL syringe, Injection for Intravenous Use, Concentration = 50 mcg/mL, Preservative Free, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor CT 06095, NDC# 70004-0200-16.
Reported: March 8, 2023 Initiated: February 24, 2023 #D-0363-2023
Product Description
Fentanyl 1,500 mcg/30 mL syringe, Injection for Intravenous Use, Concentration = 50 mcg/mL, Preservative Free, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor CT 06095, NDC# 70004-0200-16.
Reason for Recall
Subpotent Drug
Details
- Recalling Firm
- SCA Pharmaceuticals
- Units Affected
- 2125 syringes
- Distribution
- Nationwide in the US.
- Location
- Windsor, CT
Frequently Asked Questions
What product was recalled? ▼
Fentanyl 1,500 mcg/30 mL syringe, Injection for Intravenous Use, Concentration = 50 mcg/mL, Preservative Free, Rx Only, Single Dose Container, SCA Pharmaceuticals, Windsor CT 06095, NDC# 70004-0200-16.. Recalled by SCA Pharmaceuticals. Units affected: 2125 syringes.
Why was this product recalled? ▼
Subpotent Drug
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 8, 2023. Severity: Low. Recall number: D-0363-2023.
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