US Drug Recall Register
Class I · High risk Terminated Initiated Oct 5, 2020 (6 years ago)

MORPHINE-HYDROMORPHONE-BUPIVACAINE PF 13MG-19MG-2MG/ML INJECTABLE 21 mL syringe, Rx only…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Non-Sterility

What was recalled

MORPHINE-HYDROMORPHONE-BUPIVACAINE PF 13MG-19MG-2MG/ML INJECTABLE 21 mL syringe, Rx only, Med Shop 470 E. Loop 281 Longview, TX 75605

Recalling firm
Med Shop Total Care Inc.
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0712-2021

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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