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.
- Company
- Baxter Healthcare Corporation
- Recall Initiated
- March 21, 2025
- Posted
- April 15, 2025
- Recall Number
- Z-1563-2025
- Quantity
- 70627 units
- Firm Location
- Deerfield, IL
Reason for Recall
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
Distribution
Worldwide distribution.
Lot / Code Info
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
Root Cause
Device Design
Action Taken
Baxter issued an Urgent Medical Device Recall notice to its consignees on 03/21/2025 via USPS First Class Mail. The notice explained the issue, hazard involved, and requested the following: Actions to be Taken by Customers 1. Immediately locate the impacted products (see Attachment A for details) at your facility that are unopened. 2. If you received this communication directly from Baxter, acknowledge receipt by following the instructions on the enclosed Reply Form Instruction Sheet, even if you have no remaining inventory. 3. If you purchased this product from a distributor or wholesaler, please contact your supplier to arrange for the return and exchange of the affected product. Please note that responding on the Baxter customer portal is not applicable. If a response is requested by your distributor or wholesaler, please respond to them according to their instructions. 4. Please forward a copy of this communication to the Director of Nursing, and any other departments within your institution who unpack the affected product. 5. If you are a dealer, wholesaler, distributor/reseller, or original equipment manufacturer (OEM) and you have an affected product please do not distribute. Contact Baxter Technical Support for additional instructions. 6. If you are a dealer, wholesaler, distributor/reseller, or original equipment manufacturer (OEM) that distributed any affected product to other facilities, please conduct a consumer-level recall of the affected product that you distributed to customers and check the associated box on the customer portal. For general questions regarding this communication, please contact Baxter Technical Support between the hours of 8:00 am and 8:00 pm Eastern Time, Monday through Friday at 800-535-6663. Press option 2, then select option 1 or 2 for language preference, then press option 2.