FDA Device recall Z-0752-2023

Vivid S5 Ultrasound

FDA Device
Class II
ongoing
Published 2022-12-28

On 2022-12-28 the FDA classified a Class II recall of Vivid S5 Ultrasound by Ge Medical Systems, citing potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0752-2023
Classification	Class II
Status	ongoing
Initiated	2022-11-10
Published	2022-12-28
Last updated	2026-09-13 11:56 UTC
Company	Ge Medical Systems
Distribution	US

Product

Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superficial; Urology (including prostate); Transesophageal; Transrectal; Transvaginal; and Intraoperative (abdominal, thoracic, and vascular).

Reason

Potential for batteries that have not been replaced at 2 years, as recommended in the Service Manual, they can fail or possibly emit smoke, or catch fire.

Identifiers

code_info	Model Number (System ID): H45021LC (VS50873, VS51169, VS5227, VS594, VS5289, VS544, VS5155, VS50058, VS519, VS551, VS50… Model Number (System ID): H45021LC (VS50873, VS51169, VS5227, VS594, VS5289, VS544, VS5155, VS50058, VS519, VS551, VS50589, VS5286, VS5317, VS5299, VS50954, VS50940, VS560, VS50793, VS50311, VS50028, VS5125, VS50648, VS50721, VS50851, VS5300, VS5224, VS516, VS5306, VS50097, VS50154, VS50841, VS50513, VS5294, VS5151, VS50908, VS5511, VS5169, VS50746, VS50795, VS50816, VS50895, VS51008, VS50750, VS5304, VS5297, VS5495, VS50634, VS5874, VS50830, VS50931, DZ1270US01, AZ4001US03, AZ4002US01, 130083US09, 629782US01, 220909US02, 190282US07, 190282US08, 030232US18, 030232US19, 030151US07, 030151US06, 030151US05, 624025US01, 030488US01, 190226US06, 852578US02, 110009US05, 190902US02, 550020US03, 030024US01, 100029US06, 110014US31, 110014US06, 030800US16, 110019US17, VS5146VS5, VS50530VS5, VS5194VS5, VS5133VS5, VS5147VS5, VS5545VS5, 2830213, LP594207SU8, VS5176VS5, VS50166VS5, BG4607US01, BG4576US01, BG4037US08, BG4000US03, 519631VS5A, VS5907VS5, 2829006, 082438090140, 082438070046, 082438070047

code_info

Model Number (System ID): H45021LC (VS50873, VS51169, VS5227, VS594, VS5289, VS544, VS5155, VS50058, VS519, VS551, VS50…

Model Number (System ID): H45021LC (VS50873, VS51169, VS5227, VS594, VS5289, VS544, VS5155, VS50058, VS519, VS551, VS50589, VS5286, VS5317, VS5299, VS50954, VS50940, VS560, VS50793, VS50311, VS50028, VS5125, VS50648, VS50721, VS50851, VS5300, VS5224, VS516, VS5306, VS50097, VS50154, VS50841, VS50513, VS5294, VS5151, VS50908, VS5511, VS5169, VS50746, VS50795, VS50816, VS50895, VS51008, VS50750, VS5304, VS5297, VS5495, VS50634, VS5874, VS50830, VS50931, DZ1270US01, AZ4001US03, AZ4002US01, 130083US09, 629782US01, 220909US02, 190282US07, 190282US08, 030232US18, 030232US19, 030151US07, 030151US06, 030151US05, 624025US01, 030488US01, 190226US06, 852578US02, 110009US05, 190902US02, 550020US03, 030024US01, 100029US06, 110014US31, 110014US06, 030800US16, 110019US17, VS5146VS5, VS50530VS5, VS5194VS5, VS5133VS5, VS5147VS5, VS5545VS5, 2830213, LP594207SU8, VS5176VS5, VS50166VS5, BG4607US01, BG4576US01, BG4037US08, BG4000US03, 519631VS5A, VS5907VS5, 2829006, 082438090140, 082438070046, 082438070047

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0752-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.