Why it was recalled
Crystallization: Product appears to be turbid.
Product description
VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection for Intravenous Use Only), 260 mL per bag, Rx Only, This is a Compounded Drug, Hospital/Office Use Only, Apollo Care 3801 Mojave Ct, Suite 101, Columbia, MO 65202, NDC 71170-254-25
Lot numbers, UPCs & expiration codes
Lot #: AC-016402, Exp 2/12/2022
Where it was sold
MO
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-0277-2022
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 28, 2021
- FDA report date
- Dec 15, 2021
- Quantity
- 225 bags
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Apollo Care
Original FDA data
Every field from FDA enforcement report D-0277-2022, exactly as published.
Show all FDA fields
- City
- Columbia
- State
- MO
- Status
- Terminated
- Country
- United States
- Event ID
- 89011
- Address
- 3801 Mojave Ct Ste 101
- Code information
- Lot #: AC-016402, Exp 2/12/2022
- Postal code
- 65202-4042
- Report date
- Dec 15, 2021
- Product type
- Drugs
- Recall number
- D-0277-2022
- Classification
- Class II
- Recalling firm
- Apollo Care
- Product quantity
- 225 bags
- Termination date
- Dec 28, 2022
- Reason for recall
- Crystallization: Product appears to be turbid.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection for Intravenous Use Only), 260 mL per bag, Rx Only, This is a Compounded Drug, Hospital/Office Use Only, Apollo Care 3801 Mojave Ct, Suite 101, Columbia, MO 65202, NDC 71170-254-25
- Distribution pattern
- MO
- Recall initiation date
- Oct 28, 2021
- Initial firm notification
- Letter
- Center classification date
- Dec 8, 2021