Human Chorionic Gonadotropin recall: Labeling Error
Human Chorionic Gonadotropin, EP (HCG) in 5 mu. 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing…
Why was Human Chorionic Gonadotropin recalled?
Labeling: Label Error on Declared Strength; Firm states that erroneous potency information was found on the label.
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?
Lot Numbers 101751/A, Exp: 05/16, CAS: 9002-61-3; 101752/A, Exp: 05/16, CAS 9002-61-3; and 101799/A, Exp: 05/16, CAS: 9002-61-3. NDC 38779-2673-1, NDC 38779-2673-2, and NDC 38779-2673-6.
- Product
- Human Chorionic Gonadotropin, EP (HCG) in 5 mu. 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing…
- Recalling firm
- Medisca Inc.
- Quantity
- 296 units
- Distribution
- Nationwide
- Recall date
- May 7, 2014
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (drug)