Buffered Lidocaine — Class II drug recall D-0028-2017
Terminated recall by Pharmedium Services, LLC, reported 2016-10-19, distributed nationwide. Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
| Recall number | D-0028-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pharmedium Services, LLC, Lake Forest, IL, United States |
| Recall initiated | 2015-07-17 |
| Classified | 2016-10-12 |
| Reported by FDA | 2016-10-19 |
| Terminated | 2017-06-23 |
| Distributed | Nationwide (US) |
| Quantity | 10 syringes |
| Reason classes | potency, specification failure |
| Lot numbers | 15195070E |
Product
Buffered Lidocaine, 2%, In Sodium Bicarbonate 8.4%, 3 mL Total Volume in a syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2475.
Reason for recall
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0028-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.