FDA Drug recall D-0211-2017
Lidocaine HCL/ Sodium Bicarb, 1%/0.5% 0.5 mL SYR PF, packaged in a 3 cc pre-filled syringe, Rx only
- FDA Drug
- Class I
- terminated
- Published 2016-12-28
On 2016-12-28 the FDA classified a Class I recall of Lidocaine HCL/ Sodium Bicarb, 1%/0.5% 0.5 mL SYR PF, packaged in a 3 cc pre-filled syringe, Rx only by Guardian Pharmacy Services, citing non-Sterility: failed sterility test result.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0211-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2016-09-23 |
| Published | 2016-12-28 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Guardian Pharmacy Services |
| Distribution | TX |
Product
Lidocaine HCL/ Sodium Bicarb, 1%/0.5% 0.5 mL SYR PF, packaged in a 3 cc pre-filled syringe, Rx only
Reason
Non-Sterility: failed sterility test result.
Identifiers
| code_info | Lot #: 50699:00, Exp 10/04/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0211-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.