Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2
Reported: July 17, 2024 Initiated: July 3, 2024 #D-0594-2024
Product Description
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2
Reason for Recall
Subpotent Drug: reduced efficacy for epinephrine
Details
- Recalling Firm
- TAILSTORM HEALTH INC
- Units Affected
- 12,525 10 mL vials
- Distribution
- Nationwide in the USA
- Location
- Chandler, AZ
Frequently Asked Questions
What product was recalled? ▼
Lidocaine HCL Injection, USP 2% 200mg/10mL (20mg/mL) and EPINEPHRINE HCl 1:200,000, 10 ml Single Dose Vial, Rx only, Compounded drug by Medivant Healthcare, 158 S Kyrene Rd, Chandler, AZ 85226, NDC 81483-0038-0, UPC 3 81483 00380 2. Recalled by TAILSTORM HEALTH INC. Units affected: 12,525 10 mL vials.
Why was this product recalled? ▼
Subpotent Drug: reduced efficacy for epinephrine
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on July 17, 2024. Severity: Moderate. Recall number: D-0594-2024.
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