Published recall report · GlassUpdated · 11 yr ago
Hospira, Inc. recall: 1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02
1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
1% Lidocaine HCl Injection, USP, 10 mg/mL, 30 mL Vial, Single-dose Preservative Free, Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-4279-02
- Producer
- Hospira, Inc.
- Brand
- LIDOCAINE HYDROCHLORIDE
44-359-DK
- Dates on pack
- Lot #: 44-359-DK, Exp 08/01/2016
More detail
Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.
In the news
Reporting from news publishers. Follow the official notice for product advice.
No news stories about this recall yet.