Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box, Rx Only, Sandoz Inc, Princeton, NJ 08540. NDC: 0781-3299-69
Reported: January 3, 2024 Initiated: January 26, 2022 #D-0179-2024
Product Description
Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box, Rx Only, Sandoz Inc, Princeton, NJ 08540. NDC: 0781-3299-69
Reason for Recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Details
- Recalling Firm
- CARDINAL HEALTHCARE
- Units Affected
- 2 units
- Distribution
- Nationwide USA
- Location
- Dublin, OH
Frequently Asked Questions
What product was recalled? ▼
Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box, Rx Only, Sandoz Inc, Princeton, NJ 08540. NDC: 0781-3299-69. Recalled by CARDINAL HEALTHCARE. Units affected: 2 units.
Why was this product recalled? ▼
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 3, 2024. Severity: Moderate. Recall number: D-0179-2024.
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