dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.
Reported: April 30, 2025 Initiated: March 31, 2025 #D-0371-2025
Product Description
dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.
Reason for Recall
Lack of Assurance of Sterility: Leaking/damaged syringes.
Details
- Recalling Firm
- Denver Solutions, LLC DBA Leiters Health
- Units Affected
- 23,610 syringes
- Distribution
- Nationwide in the U.S.A
- Location
- Englewood, CO
Frequently Asked Questions
What product was recalled? ▼
dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg (base) per 5mL, (4 mcg (base) per mL), 5mL Single Dose syringe, Rx only, Leiters Health, 13796 Compark Blvd, Englewood, CO 80112, NDC: 71449-131-11.. Recalled by Denver Solutions, LLC DBA Leiters Health. Units affected: 23,610 syringes.
Why was this product recalled? ▼
Lack of Assurance of Sterility: Leaking/damaged syringes.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on April 30, 2025. Severity: Moderate. Recall number: D-0371-2025.
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