Lidocaine HCL/ Sodium Bicarb — Class I drug recall D-0211-2017
Terminated recall by Guardian Pharmacy Services, reported 2016-12-28, distributed in TX. Non-Sterility: failed sterility test result.
| Recall number | D-0211-2017 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Guardian Pharmacy Services, Dallas, TX, United States |
| Recall initiated | 2016-09-23 |
| Classified | 2016-12-22 |
| Reported by FDA | 2016-12-28 |
| Terminated | 2017-08-07 |
| Distributed | TX |
| Quantity | 180 syringes |
| Reason classes | sterility |
| Expiration dates | 2016-10-04 |
Product
Lidocaine HCL/ Sodium Bicarb, 1%/0.5% 0.5 mL SYR PF, packaged in a 3 cc pre-filled syringe, Rx only
Reason for recall
Non-Sterility: failed sterility test result.
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-0211-2017. 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.