Data Foundry

Medical device recalls 2025

Welch Allyn Welch Allyn Connex Spot Monitor — Class II medical device recall Z-1563-2025

Ongoing recall by Baxter Healthcare Corporation, reported 2025-04-23. Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs

Recall numberZ-1563-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmBaxter Healthcare Corporation, Deerfield, IL, United States
Recall initiated2025-03-21
Classified2025-04-15
Reported by FDA2025-04-23
Quantity70,627 units
Reason classesundeclared allergen
UPC / GTIN / UDI-DI00732094209167, 00732094209334, 00732094209372, 00732094209419, 00732094209464, 00732094209518, 00732094209570, 00732094209624, 00732094209679, 00732094209716, 00732094209792, 00732094209860, 00732094209921, 00732094210033, 00732094210712, 00732094240597, 00732094240603, 00732094322477, 00732094322491, 00732094335538, 00732094335606, 00732094335712, 00732094335781
Lot numbers24-314
Model numbers73WT-B, 74CE-B, 74CT-B, 74CX-B, 74ME-B, 74MT-B, 74MX-B, 74RE-B, 74RT-B, 75-HCA-CTB, 75-HCA-MTB, 75CE-B, 75CT-B, 75CT-BR, 75CX-B, 75ME-B, 75MT-B, 75MT-BR, 75MX-B, 75RE-B, 75RT-B, 75WE-B, 75WT-B

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 for recall

Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1563-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.