Enoxaparin Sodium Injection recall: CGMP Deviations
Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box…
Why was Enoxaparin Sodium Injection recalled?
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Batch SAH06821A
- Product
- Enoxaparin Sodium Injection, USP, 150MG/ML Single-Dose Syringes with Automatic Safety Device, For Subcutaneous Injection, Ten 1 mL Syringes per box…
- Recalling firm
- CARDINAL HEALTHCARE
- Quantity
- 2 units
- Distribution
- Nationwide USA
- Recall date
- January 3, 2024
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)