Class II · ModerateActive recall
Lidocaine Hydrochloride
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: AE3102, 031926L01, 032026A01, Exp 11/30/2026; AE5052, 052026G01, Exp 04/30/2028.
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Lack of Assurance of Sterility
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made bySportpharm LLC
| Brand name | LIDOCAINE HYDROCHLORIDE |
| Generic name | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Active ingredient(s) | LIDOCAINE HYDROCHLORIDE ANHYDROUS |
| Distributed by / for | Enovachem Pharmaceuticals, Torrance, CA 90501 |
| NDC | 85766-187-01 |
Show the full FDA record
| Full product label | Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by Enovachem Pharmaceuticals, Torrance, CA 90501, NDC: 85766-187-01. |
| Recalling firm | Asclemed USA Inc. |
| Distribution | USA Nationwide |
| Quantity | N/A |
| Recall initiated | 2026-06-08 |
| Report date | 2026-07-08 |
| Recall completed | — |
| Recall number | D-0659-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Torrance CA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.