FDA Device recall Z-0322-2025

Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System

FDA Device
Class II
ongoing
Published 2024-11-13

On 2024-11-13 the FDA classified a Class II recall of Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System by Baxter Healthcare, citing there is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0322-2025
Classification	Class II
Status	ongoing
Initiated	2024-10-11
Published	2024-11-13
Last updated	2026-09-13 11:57 UTC
Company	Baxter Healthcare
Distribution	n/a

Product

Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System; Electrocardiograph

Reason

There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.

Identifiers

code_info	Software Versions: Software Version V6.0.0 V6.2.3, Release Date 02-Jul-2015; Software Version V7.0.0, Release Date… Software Versions: Software Version V6.0.0 V6.2.3, Release Date 02-Jul-2015; Software Version V7.0.0, Release Date 02-Oct-2017 Units: 1) UDI/DI 00732094262957, Serial Numbers: 118100617841, 118250001722, 118480000511, 119140000676, 119150000331, 119180000544, 119180000545, 119180000546, 119180000547, 119180000548, 119180000549, 119180000550, 119180000551, 119340002011, 119340002012, 119460000996, 119470001912, 120110000469, 120130001657, 120160001284, 120420002132, 120420002133, 120420002134, 120420002135, 120420002136, 121330000576, 121330000577, 121330000578, 121330000579, 121330000580, 121330000581, 121330000582, 121390000797; 2) UDI/DI 00732094263046, Serial Numbers: 118460001965, 119150000243, 119390000178, 119390000179, 119500000539, 120480001168, 9069365, 121030000268, 121130001324, 121270000249, 121380000289, 121480000761, 121480000762, 121480000763, 121480000764, 121480000765, 121480000766, 121480000767, 121480000768, 121480000769, 121480000770, 121480000771, 121490

code_info

Software Versions: Software Version V6.0.0 V6.2.3, Release Date 02-Jul-2015; Software Version V7.0.0, Release Date…

Software Versions: Software Version V6.0.0 V6.2.3, Release Date 02-Jul-2015; Software Version V7.0.0, Release Date 02-Oct-2017 Units: 1) UDI/DI 00732094262957, Serial Numbers: 118100617841, 118250001722, 118480000511, 119140000676, 119150000331, 119180000544, 119180000545, 119180000546, 119180000547, 119180000548, 119180000549, 119180000550, 119180000551, 119340002011, 119340002012, 119460000996, 119470001912, 120110000469, 120130001657, 120160001284, 120420002132, 120420002133, 120420002134, 120420002135, 120420002136, 121330000576, 121330000577, 121330000578, 121330000579, 121330000580, 121330000581, 121330000582, 121390000797; 2) UDI/DI 00732094263046, Serial Numbers: 118460001965, 119150000243, 119390000178, 119390000179, 119500000539, 120480001168, 9069365, 121030000268, 121130001324, 121270000249, 121380000289, 121480000761, 121480000762, 121480000763, 121480000764, 121480000765, 121480000766, 121480000767, 121480000768, 121480000769, 121480000770, 121480000771, 121490

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0322-2025%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.