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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Device
Medical Devices/Monitoring Devices

Welch Allyn Medical Monitors and Equipment Recalled for Battery Fire Risk

Agency Publication Date: April 14, 2025
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Summary

Baxter Healthcare Corporation is recalling 384,353 units of Welch Allyn medical equipment, including the Connex Vital Signs Monitor (CVSM), Accessory Power Management Stands, and CP150 Electrocardiographs. This recall follows customer reports of battery-related fires caused by the use of unapproved, third-party aftermarket batteries that are not authorized by Baxter. While specific injury counts were not provided in the initial notice, the potential for fire poses a significant safety risk to patients, healthcare staff, and medical facilities. If you use this equipment, contact Baxter Healthcare Corporation or your authorized medical distributor immediately to ensure your devices are equipped with approved batteries.

Risk

The use of non-Baxter approved batteries in these devices can lead to battery failure and internal fires. These fires can cause severe burns, smoke inhalation, and damage to clinical environments, potentially disrupting critical patient monitoring or care.

What You Should Do

  1. This recall affects Welch Allyn Connex Vital Signs Monitors (CVSM), Welch Allyn CONNEX Accessory Power Management Stands, and Welch Allyn CP150 Electrocardiographs manufactured by Baxter Healthcare Corporation.
  2. Identify your device by looking for the product codes and UDI-DI numbers on the manufacturing label located on the rear or bottom of the unit. This recall affects a wide range of model variants across all three product lines. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device immediately if you suspect or confirm it is utilizing an unapproved, third-party aftermarket battery.
  4. Contact Baxter Healthcare Corporation or your authorized medical distributor to arrange for a return, replacement, or to obtain a Baxter-approved battery for your device.
  5. Call the FDA Consumer Complaint hotline at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Welch Allyn Connex Vital Signs Monitor (CVSM)
Model / REF (427):
67MCTX-4
67MCTX-6
67MCTX-B
67MCXP-B
67MCXX-B
67MREP-B
67MREX-B
67MRTP-B
67MRTX-B
67MRXP-4
67MRXP-B
67MRXX-B
67MSTP-6
67MSTP-B
67MSTX-6
67MSTX-B
67MXDX-B
67MXEP-2
67MXEP-4
67NCEP-2
67NCEP-6
67NCEP-B
67NCEX-4
67NCTP-B
67NCTP-B-ECG3A
67NCTX-B
67NCXP-2
67NCXP-6
67NCXP-B
67NCXX-4
67NCXX-6
67NCXX-B
67NSEP-B
67NSTP-6
67NSTW-B
67NSTX-B
67NSXX-B
67NXDX-B
67NXEP-2
67NXEP-4
67NXEP-6
67NXEP-B
67NXEW-2
67NXEX-2
67NXEX-4
67NXEX-6
67NXEX-7
67NXEX-B
67NXTP-2
67NXTP-4
Serial Numbers:
All Serial Numbers
UDI (427):
00732094193787
00732094194654
00732094151367
00732094151350
00732094151343
00732094151336
00732094151329
00732094151312
00732094151305
00732094193640
00732094151299
00732094151282
00732094194548
00732094177541
00732094194531
00732094177558
00732094249163
00732094193619
00732094193602
00732094193497
00732094194449
00732094151213
00732094193466
00732094151190
00732094323771
00732094151183
00732094193411
00732094194401
00732094151176
00732094193381
00732094194395
00732094151169
00732094189339
00732094194364
00732094206678
00732094177503
00732094177534
00732094249149
00732094193374
00732094193367
00732094194326
00732094151152
00732094206609
00732094193350
00732094193343
00732094194319
00732094224795
00732094151145
00732094193336
00732094193329
Product: Welch Allyn CONNEX Accessory Power Management Stand
Model / REF:
7000-APM
75-HCA-CTB
75-HCA-MTB
Serial Numbers:
All Serial Numbers
UDI:
00732094210613
00732094240597
00732094240603
Product: Welch Allyn CP150 Electrocardiograph
Model / REF (80):
CP150-2ES2
CP150-2FR2
CP150-2FR5
CP150-2NL2
CP150-2PT2
CP150-2SV2
CP150-3ENB
CP150-3ESB
CP150-4DE2
CP150-4EN2
CP150-4EN4
CP150-4PT2
CP150A-1EN2
CP150A-1EN4
CP150A-1EN66
CP150A-1ENB
CP150A-1ENBR
CP150A-1ESB
CP150A-1FRB
CP150A-2DE2
CP150A-2DE5
CP150A-2EN2
CP150A-2EN3
CP150A-2EN4
CP150A-2EN7
CP150A-2ES2
CP150A-2FR2
CP150A-2FR5
CP150A-2NL2
CP150A-2NO2
CP150A-2SV2
CP150A-3BPZ
CP150A-3EN2
CP150A-3EN3
CP150A-3EN4
CP150A-3ENB
CP150A-3ES2
CP150A-3ESB
CP150A-3ZHC-CN
CP150A-4BPZ
CP150A-4DE2
CP150A-4EN2
CP150A-4EN4
CP150A-4ES2
CP150A-4FR5
CP150A-4PT2
CP150A-4ZHC-CN
CP150AD-1ENB
CP150AD-2DE2
CP150AD-2ES2
Serial Numbers:
All Serial Numbers
UDI (80):
00732094192131
00732094192124
00732094192117
00732094192100
00732094192087
00732094192070
00732094179705
00732094179682
00732094192063
00732094179675
00732094179668
00732094192025
00732094185157
00732094185140
00732094179644
00732094177633
00732094322415
00732094192230
00732094179637
00732094192018
00732094192001
00732094177626
00732094179620
00732094177619
00732094191998
00732094191981
00732094191974
00732094191967
00732094191950
00732094191943
00732094191929
00732094212938
00732094179613
00732094179606
00732094184815
00732094179590
00732094179583
00732094177602
00732094213515
00732094212952
00732094191912
00732094177596
00732094177589
00732094177572
00732094189186
00732094189179
00732094213539
00732094237580
00732094237573
00732094237559

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96478
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Authorized Medical Distributors; Baxter Healthcare Corporation
Manufactured In: United States
Units Affected: 3 products (228,412 units; 114,202 units; 41,739 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.