---
title: "Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 7... — FDA record Z-1563-2025 | Is It on Recall"
description: "Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs."
url: https://isitonrecall.com/recall/fda-device-z-1563-2025-welch-allyn-welch-allyn-connex-spot-monitor-product-code-part-numbers-1-73wt-b-2-74ce-b-3-74ct-b-4-7/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74CX-B; ... — FDA record Z-1563-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Mar 21, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74CX-B; 5) 74ME-B; 6) 74MT-B; 7) 74MX-B; 8) 74RE-B; 9) 74RT-B; 10) 75CE-B; 11) 75CT-B; 12) 75CT-BR; 13) 75CX-B; 14) 75-HCA-CTB; 15) 75-HCA-MTB; 16) 75ME-B; 17) 75MT-B; 18) 75MT-BR; 19) 75MX-B; 20) 75RE-B; 21) 75RT-B; 22) 75WE-B; 23) 75WT-B.
- **Reason**: Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
- **Classification**: Class II
- **Recalling firm**: Baxter Healthcare Corporation
- **Quantity**: 70627 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1563-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1563-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 1) Product Code/Part # 73WT-B, UDI/DI 00732094210033; 2) Product Code/Part # 74CE-B, UDI/DI 00732094209921; 3) Product Code/Part # 74CT-B, UDI/DI 00732094209860; 4) Product Code/Part # 74CX-B, UDI/DI 00732094209792; 5) Product Code/Part # 74ME-B, UDI/DI 00732094209716; 6) Product Code/Part # 74MT-B, UDI/DI 00732094209679; 7) Product Code/Part # 74MX-B, UDI/DI 00732094209624; 8) Product Code/Part # 74RE-B, UDI/DI 00732094335781; 9) Product Code/Part # 74RT-B, UDI/DI 00732094335712; 10) Product Code/Part # 75CE-B, UDI/DI 00732094209570; 11) Product Code/Part # 75CT-B, UDI/DI 00732094209518; 12) Product Code/Part # 75CT-BR, UDI/DI 00732094322491; 13) Product Code/Part # 75CX-B, UDI/DI 00732094209464; 14) Product Code/Part # 75-HCA-CTB, UDI/DI 00732094240597; 15) Product Code/Part # 75-HCA-MTB, UDI/DI 00732094240603; 16) Product Code/Part # 75ME-B, UDI/DI 00732094209419; 17) Product Code/Part # 75MT-B, UDI/DI 00732094209372; 18) Product Code/Part # 75MT-BR, UDI/DI 00732094322477; 19) Product Code/Part # 75MX-B, UDI/DI 00732094209334; 20) Product Code/Part # 75RE-B, UDI/DI 00732094335606; 21) Product Code/Part # 75RT-B, UDI/DI 00732094335538; 22) Product Code/Part # 75WE-B, UDI/DI 00732094210712; 23) Product Code/Part # 75WT-B, UDI/DI 00732094209167; Lot Number 24-314 & lower |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Apr 23, 2025
- **Recall initiation date**: Mar 21, 2025
- **Center classification date**: Apr 15, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1563-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Baxter Healthcare Corporation records](https://isitonrecall.com/brand/baxter-healthcare-corporation/)