Asclemed USA Inc. recalls
Every recall we track for Asclemed USA Inc. — 4 in all, all from 2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Asclemed USA Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 3 | 1 | 4 |
Most common reasons for Asclemed USA Inc. recalls
What to do if you have a recalled Asclemed USA Inc. product
- Match the NDC and lot number on your bottle or box to the recall.
- Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first.
- Report side effects to FDA MedWatch.
All Asclemed USA Inc. recalls
3 shown- Lower riskDrug
Asclemed USA Inc. recalls Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed
Asclemed recalls Lidolog Kit (2% Lidocaine injection) due to label wrap covering barcode, making scanning difficult. Affected units have specific lot and expiration dates.
AsclemedJul 15, 2026 - Lower riskDrug
Asclemed USA Inc. recalls Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only, Distributed by
Asclemed recalls Accucaine 1% Lidocaine injection due to lack of sterility assurance. This may cause infections if used improperly. Contact the manufacturer for details.
AsclemedJun 8, 2026 - UnratedDrug
Asclemed USA Inc. recalls Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC
Asclemed USA recalls 30mg Duloxetine DR Capsules due to nitrosamine impurity exceeding FDA limits. Consumers should check product labels for NDC 76420-634-30 and lot numbers 050725F-30 or 050725G-30.
Asclemed USAMay 14, 2026
Asclemed USA Inc. recall questions
How many recalls has Asclemed USA Inc. had?
4 recalls from Asclemed USA Inc. are on record with U.S. safety agencies, from 2026.
What is the most recent Asclemed USA Inc. recall?
Asclemed USA Inc. recalls Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only, Distributed, dated Jul 15, 2026. Every Asclemed USA Inc. recall is listed on this page, newest first.
Why are Asclemed USA Inc. products recalled?
The most common reasons on record: Lack of Assurance of Sterility (2).
What should I do if I have a recalled Asclemed USA Inc. product?
Match the NDC and lot number on your bottle or box to the recall. Don’t stop a prescription on your own — ask your pharmacist or doctor for a replacement first. Report side effects to FDA MedWatch.
How do I get alerts for new Asclemed USA Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.