Akorn, Inc. Recall: Lidocaine Hydrochloride Jelly USP, 2%, Packaged as (a) 5 mL tube (NDC
Akorn, Inc. Recall: Lidocaine Hydrochloride Jelly USP, 2%, Packaged as (a) 5 mL tube (NDC is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Akorn, Inc.; Product: Lidocaine Hydrochloride Jelly USP, 2%, Packaged as (a) 5 mL tube (NDC 17478-711-10) x10 per box NDC 17478-711-31; (b) 30 mL tu
| Recalling firm | Akorn, Inc. |
|---|---|
| Product | Lidocaine Hydrochloride Jelly USP, 2%, Packaged as (a) 5 mL tube (NDC 17478-711-10) x10 per box NDC 17478-711-31; (b) 30 mL tube NDC 17478-711-30; Rx only, Manufactured by: Akorn, Inc., Lake Forest, Il 60045. |
| Reason for recall | CGMP Deviations: |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide in the USA |
| Recall initiated | 20221013 |
| Recall number | D-0143-2023 |
| Category | drug |
| State | IL |
| Country | United States |
$29/mo
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