FDA Drug recall D-1234-2014
1% Lidocaine HCl Injection, USP, 10 mg/mL, NDC 0409-4276-01, Hospira, Inc., Lake Forest, IL 60045
- FDA Drug
- Class I
- terminated
- Published 2014-04-23
On 2014-04-23 the FDA classified a Class I recall of 1% Lidocaine HCl Injection, USP, 10 mg/mL, NDC 0409-4276-01, Hospira, Inc., Lake Forest, IL 60045 by Hospira, citing presence of Particulate Matter: Oxidized stainless steel found in vial of 1% Lidocaine Hydrochloride Injection, USP.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1234-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-09-16 |
| Published | 2014-04-23 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Hospira |
| Distribution | US |
Product
1% Lidocaine HCl Injection, USP, 10 mg/mL, NDC 0409-4276-01, Hospira, Inc., Lake Forest, IL 60045.
Reason
Presence of Particulate Matter: Oxidized stainless steel found in vial of 1% Lidocaine Hydrochloride Injection, USP.
Identifiers
| ndc | 0409-4713-12 |
|---|---|
| ndc | 0409-4713-26 |
| ndc | 0409-4713-02 |
| ndc | 0409-4713-72 |
| ndc | 0409-4713-62 |
| ndc | 0409-4713-75 |
| ndc | 0409-4713-65 |
| ndc | 0409-4713-42 |
| ndc | 0409-4713-25 |
| ndc | 0409-4713-32 |
| ndc | 0409-4278-16 |
| ndc | 0409-4278-01 |
| ndc | 0409-4279-16 |
| ndc | 0409-4279-02 |
| ndc | 0409-4776-10 |
| ndc | 0409-4776-01 |
| ndc | 0409-4282-11 |
| ndc | 0409-4282-25 |
| ndc | 0409-4282-01 |
| ndc | 0409-4282-12 |
| ndc | 0409-4282-02 |
| ndc | 0409-4277-16 |
| ndc | 0409-4277-01 |
| ndc | 0409-4277-17 |
| ndc | 0409-4277-02 |
| ndc | 0409-4276-16 |
| ndc | 0409-4276-01 |
| ndc | 0409-4276-17 |
| ndc | 0409-4276-02 |
| ndc | 0409-4275-16 |
| ndc | 0409-4275-01 |
| code_info | Lot #25090DK; Exp 01/15 |
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-1234-2014%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.