Drug recall D-1335-2022
Product
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
Reason for recall
Defective Delivery System: An incorrect 10 mL (12 mL) Luer (slip) syringe packaged in one lot of Zynrelef 400 mg/12 mg kit
Lots and codes
Lot #: 01126739, Exp 7/31/2023
Recall details
- Recalling firm
- HERON THERAPEUTICS, INC., San Diego, CA
- Quantity
- 1790 kits
- Distribution
- U.S.A. Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- August 2, 2022
- Terminated
- September 29, 2023
Related products
- Zynrelef – drug information
- NDC 47426-503 Zynrelef · Bupivacaine 200 mg/7mL; Meloxicam 6 mg/7mL · Heron Therapeutics, Inc.
- NDC 47426-501 Zynrelef · Bupivacaine 400 mg/14mL; Meloxicam 12 mg/14mL · Heron Therapeutics, Inc.