Asclemed USA recalls
Asclemed USA has 10 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 29 Jul 2026. 5 are still ongoing. 4 were reported in the last 12 months. The most frequent reason is potency & assay.
Total recalls10since 2018
Last 12 months4reported
Class I220% of total
Ongoing5latest 29 Jul 2026
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 2 20%Class II 6 60%Class III 2 20%
Why asclemed usa is recalled
Product types
Brands
By year
Ongoing asclemed usa recalls
5 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Lidolog Kit, Kit Contains: Lidocaine HCl Injection recalledLidolog Kit | Asclemed USA | Other | TN |
| Drug | CLASS II | Lidocaine HCl Injection USP, 1% (10 mg/mL) single dose ampule recalledLidocaine Hydrochloride | Asclemed USA | Sterility | Nationwide |
| Drug | CLASS II | Accucaine, Kit contains: Lidocaine HCl Injection recalledAccucaine | Asclemed USA | Sterility | Nationwide |
| Drug | CLASS II | Duloxetine DR Capsules, 30 mg, Rx, Relabeled recalled by Asclemed USADuloxetine | Asclemed USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS III | Asclemed USA products recalled | Asclemed USA | Other | AL, CA, LA |
All asclemed usa recalls, newest first
10 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.