Apollo Care: Drug Recall
Recall #D-0487-2023 · 02/08/2023
Class II: Risk
Recall Details
- Recall Number
- D-0487-2023
- Classification
- Class II
- Product Type
- Drug
- Recalling Firm
- Apollo Care
- Status
- Ongoing
- Date Initiated
- 02/08/2023
- Location
- Columbia, MO, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 215 bags
Reason for Recall
Lack of assurance of sterility: Suspected microbial growth present on external label packaging.
Product Description
Fentanyl 500mcg (2mcg/mL) and Ropivacaine HCl 250mg (1mg/mL) added to 250mL 0.9% Sodium Chloride, For Epidural Use Only, Rx only, 3801 Mojave Ct. Suite 101, Columbia, MO 65202, NDC 71170-950-25
Distribution Pattern
MO
Other Recalls by Apollo Care
- Class II: Risk 10/28/2021
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.