Why it was recalled
Lack Of Assurance Of Sterility.
Product description
oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44
Lot numbers, UPCs & expiration codes
Lot: 20170912@13 BUD: 10/22/2017
Where it was sold
Nationwide in the United States
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-0065-2018
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 19, 2017
- FDA report date
- Nov 8, 2017
- Quantity
- 450 bags
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- SCA Pharmaceuticals, LLC
Original FDA data
Every field from FDA enforcement report D-0065-2018, exactly as published.
Show all FDA fields
- City
- Little Rock
- State
- AR
- Status
- Terminated
- Country
- United States
- Event ID
- 78320
- Address
- 8821 Knoedl Ct
- Code information
- Lot: 20170912@13 BUD: 10/22/2017
- Postal code
- 72205-4600
- Report date
- Nov 8, 2017
- Product type
- Drugs
- Recall number
- D-0065-2018
- Classification
- Class II
- Recalling firm
- SCA Pharmaceuticals, LLC
- Product quantity
- 450 bags
- Termination date
- May 1, 2019
- Reason for recall
- Lack Of Assurance Of Sterility.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- oxyTOCIN 30 units added to Lactated Ringers 500 mL Bag, Rx Only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205, NDC 70004-0086-44
- Distribution pattern
- Nationwide in the United States
- Recall initiation date
- Oct 19, 2017
- Initial firm notification
- Letter
- Center classification date
- Nov 2, 2017