Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Zynrelef (bupivacaine and meloxicam) Recalled by HERON THERAPEUTICS, INC. Due to Defective Delivery System: An incorrect 10 mL (12...
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 HERON THERAPEUTICS, INC. directly.
Affected Products
Zynrelef (bupivacaine and meloxicam), 400 mg bupivacaine and 12 mg meloxicam single dose application, packaged in a kit, Rx only, Manufactured for Heron Therapeutics, Inc., San Diego, CA, NDC 47426-301-02
Quantity: 1790 kits
Why Was This Recalled?
Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe packaged in one lot of Zynrelef 400 mg/12 mg kit
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About HERON THERAPEUTICS, INC.
HERON THERAPEUTICS, INC. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report