RScribe recallZ-0322-2025 · Baxter Healthcare Corporation · initiated Oct 11, 2024
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
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Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
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.
FDA root cause category: Software design
What the company is doing
Baxter issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 10/11/2024 via USPS First Class Mail. The notice explained the issue, potential hazard to the patient, and provided instructions for the to the system IT administrator to correct the issue which is already available in the current version of software.
Recall details
- Recall number
- Z-0322-2025
- Status
- Open, Classified
- Initiated by the company
- Oct 11, 2024
- Posted by the FDA
- Nov 7, 2024
- Recalling firm
- Baxter Healthcare Corporation
- Quantity
- 399 units
- Product code
- DPS
- FDA submissions
- K120865
- Distribution
- Worldwide distribution.
Product description
Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System; Electrocardiograph
Code information (models, lots, serial numbers)
Show the full code information (6k characters)
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, 121490000809, 121490000810, 121490000811, 121370002215, 122020001003, 122020001004, 122020001005, 122020001006, 122020001007, 122020001008, 122020001009, 122020001010, 122020001011, 122020001012, 122020001013, 122050001754, 122050001755, 122050001756, 122050001757, 122050001758, 122050001759, 122040000338, 122040000339, 122040000341, 122050000662, 122050000667, 122120002583, 122120002584, 122120002585, 122120002586, 122120002587, 122120002588, 122120002589, 122120002590, 122120002591, 122120002592, 122120002593, 122120002594, 122160000170, 122160000171, 122160000172, 122200000716, 122200000717, 122200000718, 122200000719, 123060000574, 123060000575, 123060000576, 123060000577, 123060000578, 123060000579, 123060000580, 123060000581, 123060000582, 123100001462, 123100001463, 122450001687, 122450001690, 122450001691, 122450001693, 122120002594, 122200000716, 123060000576, 123060000578, 123060000581, 123060000582, 123320000688, 123320000689; 3) UDI/DI 00732094263107, Serial Numbers: 116440534586, 116440534587, 116440534588, 116440534589, 116440534590, 116440534591, 116440534592, 116440534593, 116440534594, 116440534595, 116440534596, 116440534597, 116440534598, 116440534599, 116440534600, 117010549214, 117010549215, 117010549216, 117010549217, 117010549218, 117010549219, 117010549220, 117010549221, 117010549222, 117010549223, 117130559079, 117130559080, 117130559081, 117130559082, 117130559083, 117130559084, 117130559085, 117130559086, 117130559087, 117130559088, 117130559089, 117130559090, 117130559091, 117130559092, 117130559093, 117270577247, 117270577248, 117270577249, 117270577250, 117270577251, 117270577252, 117270577253, 117270577254, 117270577255, 117270577256, 117360584807, 117360584808, 117360584809, 117360584810, 117360584811, 117360584812, 117360584813, 117360584814, 117360584815, 117360584816, 118110619366, 118110619367, 118110619368, 118110619369, 118110619370, 118110619371, 118110619372, 118110619373, 118110619374, 118110619375, 118450001287, 118450001288, 118450001289, 118450001290, 118450001291, 118450001292, 118450001293, 118450001294, 118450001295, 118450001296, 119240000205, 119240000206, 119240000207, 119240000208, 119240000209, 119240000210, 119240000211, 119240000212, 119240000213, 119240000214, 119240000216, 119240000217, 119240000218, 119240000219, 119240000220, 119240000221, 119240000222, 119240000223, 119240000224, 119240000225, 119300001280, 119300001281, 119300001282, 119300001283, 119300001284, 119300001285, 119300001286, 119300001287, 119300001288, 119300001289, 121030000675, 121030000676, 121030000677, 121030000678, 121030000679, 121030000680, 121030000681, 121030000682, 121030000683, 121030000684, 121040000881, 121040000882, 121040000883, 121040000884, 121040000885, 121040000886, 121040000887, 121040000888, 121040000889, 121040000890, 121060000036, 121060000037, 121060000038, 121060000039, 121060000040, 121060000041, 121060000042, 121060000043, 121060000044, 121060000045, 121410001269, 121410001270, 121410001271, 121410001272, 121410001273, 121410001274, 121410001275, 121410001276, 121410001277, 121410001278, 121410001279, 121410001280, 121410001281, 121410001282, 121410001283, 121410001284, 121410001285, 121410001286, 121410001287, 121410001288, 122280000939, 122280000940, 122280000941, 122280000942, 122280000943, 122280000944, 122280000945, 122280000946, 122280000947, 122280000948, 122280000949, 122280000950, 122280000951, 122280000952, 122280000953, 122280000954, 122280000955, 122280000956, 122280000957, 122280000958, 122280000959, 122280000960, 122280000961, 122280000962, 122280000963, 122280000964, 122280000965, 122280000966, 122280000967, 122280000968, 122520001054, 122520001055, 122520001056, 122520001057, 122520001058, 122520001059, 122520001060, 122520001061, 122520001062, 122520001063, 123010000269, 123010000270, 123010000271, 123010000272, 123010000273, 123010000274, 123010000275, 123010000276, 123010000277, 123010000278, 122520001054; 4) UDI/DI 00732094263138, Serial Numbers: 1, 2; 5) UDI/DI 00732094263152, Serial Numbers: 117500601521; 6) UDI/DI 00732094263169, Serial Numbers: 118120622041, 118120622040, 118120622039, 118120622038, 118120622037, 118120622036, 118120622035, 118120622034, 118120622033, 118120622032; 7) UDI/DI 00812345027822, Serial Numbers: 116270501517, 117270576947; 8) UDI/DI 00812345027839, Serial Numbers: 116270499720, 116290516803, 116480540314, 117050553486, 117050553487, 117110556359, 117170566163, 117170566164, 117170566165, 117170566166, 117170566167, 117170566168, 117170566169, 117170566171, 117170566172, 117170566170, 117340583183, 117340583184, 117340583185, 117340583186, 117340583187, 117340583188, 117340583189, 117340583190, 117340583191, 117340583192, 117350584681, 116270499720; 9) UDI/DI 00817655020280, Serial Numbers: 116420532965, 116450536831, 116460538001, 117010549242, 117260576252, 117260576918, 117430592085, 117430592086, 117430592087, 117430592088, 117430592083; 10) UDI/DI 00817655021362, Serial Numbers: 117130560315, 117130560316, 117130560317; 11) UDI/DI 00817655022246, Serial Numbers: 118390000403; 12) UDI/DI none, Serial Numbers: 117220571712, 117290578777, 117290578778, 117290578779, 117290578780, 117290578781, 117290578782
Devices named in this recall
11 devices in the FDA device registry whose identifier appears in the recall's code information.
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- Welch Allyn, Inc. 901127Welch Allyn, Inc. · Electrocardiograph1 recall0 reports
- RScribe RSCRIBE-6CC-AXAABMortara Instrument, Inc. · Electrocardiograph1 recall0 reports
- RScribe RSCRIBE-6CC-XXAABMortara Instrument, Inc. · Electrocardiograph1 recall0 reports
- RScribe RSCRIBE-6AC-AXAABMortara Instrument, Inc. · Electrocardiograph1 recall0 reports
- RScribe RSCRIBE-6EC-XXDXBMortara Instrument, Inc. · Electrocardiograph1 recall0 reports
- RScribe RSCRIBE-6AC-XXAABMortara Instrument, Inc. · Electrocardiograph1 recall0 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 95559).
- Z-0320-2025 · Open, ClassifiedHillrom Welch Allyn HScribe Holter System; ambulatory monitoring
- Z-0321-2025 · Open, ClassifiedHillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test
- Z-0323-2025 · Open, ClassifiedHillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph
- Z-0324-2025 · Open, ClassifiedHillrom Welch Allyn Diagnostic Cardiology Suite (formerly Connex Cardio); Diagnostic spirometer
- Z-0325-2025 · Open, ClassifiedHillrom Welch Allyn XScribe Cardiac Stress Testing System; Programmable Diagnostic Computer
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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