Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
0.5% Bupivacaine Hydrochloride Injection Recalled by PFIZER, INC Due to Labeling: Label Mix-Up: some vials labeled to contain...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact PFIZER, INC directly.
Affected Products
0.5% Bupivacaine Hydrochloride Injection, USP, 150 mg/30 mL (5 mg/mL), 30 mL Single-dose Teartop Vials (NDC 0409-1162-19), packaged in 25 vials per tray (NDC 0409-1162-02), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA.
Quantity: 163,957 vials
Why Was This Recalled?
Labeling: Label Mix-Up: some vials labeled to contain 0.5% Bupivacaine Hydrochloride Injection, USP may contain 1% Lidocaine HCl Injection, USP and some vials labeled to contain 1% Lidocaine HCl Injection, USP may contain 0.5% Bupivacaine Hydrochloride Injection, USP
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PFIZER, INC
PFIZER, INC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report