DrugJun 7, 2023
Akorn Levofloxacin Injection 500mg/20 mL (25 mg/mL), For Intravenous Infusion recall — FDA D-0818-2023
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Class IIFDA: OngoingAkorn, Inc.
June 2023 recalls — page 15
These records include useful source details for the selected month.
VehicleJun 7, 2023
Sportage power assist recall — NHTSA campaign 23V410000
Kia America, Inc. (Kia) is recalling certain 2023 Sportage vehicles. The brake booster diaphragm may become misaligned and cause an internal vacuum leak, which can result in a loss of power…
power assistKia America, Inc.
VehicleJun 1, 2023
Ascent lower arm recall — NHTSA campaign 23V392000
Subaru of America, Inc. (Subaru) is recalling certain 2023 Ascent vehicles. The left or right front lower control arm may have an improperly tightened ball joint castle nut which can result…
lower armSubaru of America, Inc.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.