Why it was recalled
Subpotent drug.
Product description
Vasopressin 20 Units added to 0.9% Sodium Chloride 100 mL Rx Only, Single Dose Container, SCA Pharmaceuticals 8821 Knoedl Ct. Little Rock, AR 72205 Bar Code 70004093232
Lot numbers, UPCs & expiration codes
Lots: 1120025012 BUD: 01/13/2021, 1120025015 BUD: 01/15/2021, 1120025272 BUD: 01/28/2021
Where it was sold
Distributed Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0171-2021
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Dec 14, 2020
- FDA report date
- Dec 30, 2020
- Quantity
- 654 bags
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- SCA Pharmaceuticals, Inc.
Original FDA data
Every field from FDA enforcement report D-0171-2021, exactly as published.
Show all FDA fields
- City
- Little Rock
- State
- AR
- Status
- Terminated
- Country
- United States
- Event ID
- 86982
- Address
- 8821 Knoedl Ct
- Code information
- Lots: 1120025012 BUD: 01/13/2021, 1120025015 BUD: 01/15/2021, 1120025272 BUD: 01/28/2021
- Postal code
- 72205-4600
- Report date
- Dec 30, 2020
- Product type
- Drugs
- Recall number
- D-0171-2021
- Classification
- Class II
- Recalling firm
- SCA Pharmaceuticals, Inc.
- Product quantity
- 654 bags
- Termination date
- Sep 23, 2021
- Reason for recall
- Subpotent drug.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Vasopressin 20 Units added to 0.9% Sodium Chloride 100 mL Rx Only, Single Dose Container, SCA Pharmaceuticals 8821 Knoedl Ct. Little Rock, AR 72205 Bar Code 70004093232
- Distribution pattern
- Distributed Nationwide in the USA
- Recall initiation date
- Dec 14, 2020
- Initial firm notification
- Letter
- Center classification date
- Dec 21, 2020