Sterile Diluent recall: CGMP Deviations
Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin Lispro Injection u-100, 10 mL…
Why was Sterile Diluent recalled?
CGMP Deviations
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 number: D608951C, exp 4/10/2025
- Product
- Sterile Diluent, HUMALOG U-100 (insulin lispro injection), HUMULIN R U-100 REGULAR (insulin human injection), Insulin Lispro Injection u-100, 10 mL…
- Recalling firm
- Eli Lilly & Company
- Quantity
- 700 vials
- Distribution
- Nationwide USA
- Recall date
- April 24, 2024
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)