Bupivacaine Hydrochloride: 10 recalls on record

Recalled by 1 agency: FDA (10).

First recall on record: October 16, 2013. Most recent: April 22, 2026.

Risk classification: Class I: 3 · Class II: 7

Most recent recalls

DateAgencyProduct
April 22, 2026FDABupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP (15 mg/2 mL) (7.5 mg/mL)…D-0530-2026
June 15, 2022FDABupivacaine Hydrochloride, USP 0.5% (5mg/mL), 25 vials x 50 mL per box, Rx only, MFG: Pfi…D-1095-2022
June 15, 2022FDABupivacaine HCl Injection, single dose vial, Preservative Free 0.5%, 10mL (25/ct), Rx onl…D-0998-2022
December 28, 2016FDABupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Pres…D-0218-2017
September 24, 2014FDABupivacaine HCl Inj., USP, 0.5% (5 mg/mL), 30 mL Single-dose Preservative-Free, For Nerve…D-1588-2014
March 12, 2014FDABupivacaine HCl Inj. USP, 0.5% (5 mg/mL), 30 mL Single-dose Preservative Free Vial, Rx On…D-1147-2014
January 8, 2014FDA0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 50 mL, Multiple-dose Fliptop Vial, R…D-395-2014
December 25, 2013FDA0.75% Bupivacaine HCl Injection, USP, 7.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake F…D-381-2014
December 25, 2013FDA0.25% Bupivacaine HCl Injection, USP, 2.5 mg/mL, 30 mL, Single-dose, Hospira Inc., Lake F…D-380-2014
October 16, 2013FDA0.5% Bupivacaine HCl and Epinephrine 1:200,000 Inj., 10 mL, Single-Dose Vial, NDC 0409-90…D-66295-001

Questions about this brand

How many recalls does Bupivacaine Hydrochloride have?
Recalert has 10 U.S. recalls on record for Bupivacaine Hydrochloride, published between October 16, 2013 and April 22, 2026.
What was the most recent Bupivacaine Hydrochloride recall?
FDA recall D-0530-2026, published April 22, 2026: Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection, USP (15 mg/2 mL) (7.5 mg/mL) ampules, Rx only, Manufactured by: Houns Co., Ltd, 100, Bio valley, Je-cheor-Si, Chungcheongbuk-dc, Korea, ND…
Which agencies have recalled Bupivacaine Hydrochloride products?
Bupivacaine Hydrochloride products appear in recalls from: FDA (10).

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