CLASS II ONGOING Device recall · Reported 23 Apr 2025 · FDA Enforcement Report

Welch Allyn Connex Accessory Power Management Stand recalled

Baxter Healthcare is recalling Welch Allyn Connex Accessory Power Management Stand, distributed nationwide in the US. The recall was initiated on 24 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Serial Numbers. Product Code: 7000-APM, UDI-DI: 00732094210613; Product Code: 75-HCA-CTB, UDI-DI: 00732094240597; Product Code: 75-HCA-MTB, UDI-DI: 00732094240603;

Quantity recalled114,202 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1559-2025
FDA event ID: 96478
Recalling firm: Baxter Healthcare, Deerfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 24 Mar 2025
FDA classified: 14 Apr 2025
Reported: 23 Apr 2025
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Hidden Drug Ingredients
Device type: Other Medical Devices

Timeline

24 Mar 2025	Recall initiated by company
14 Apr 2025	Classified by FDA	+21 days
23 Apr 2025	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

Welch Allyn CONNEX Accessory Power Management Stand:

Where it was distributed

Worldwide - US Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

Which lots are affected?

All Serial Numbers. Product Code: 7000-APM, UDI-DI: 00732094210613; Product Code: 75-HCA-CTB, UDI-DI: 00732094240597; Product Code: 75-HCA-MTB, UDI-DI: 00732094240603;

Where was it sold?

Worldwide - US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

2 other products · FDA event 96478

This product is part of a recall event; the main page for the event is Welch Allyn Connex Vital Signs Monitor (CVSM) recalled.

Reported	Class	Recall	Company	Reason	Where
23 Apr 2025	CLASS II	Welch Allyn Connex Vital Signs Monitor (CVSM) recalled	Baxter Healthcare	Hidden Drug Ingredients	Nationwide
23 Apr 2025	CLASS II	Welch Allyn CP150 Electrocardiograph recalled by Baxter Healthcare	Baxter Healthcare	Hidden Drug Ingredients	Nationwide

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