Product Recall  from Baxter Healthcare Corporation

Baxter Healthcare Corporation is issuing a voluntary product recall for reusable blood pressure cuffs because the product is labeled “not made with natural rubber latex,” however, there is a latex-containing rubber band located around the product instructions for use (IFU). Baxter is requesting the return of unopened affected blood pressure cuffs in their packaging.

Actions to be Taken by Dealers, Wholesalers, Distributors/Resellers, or Original Equipment Manufacturers (OEM)

1. 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 at the phone number below for additional instructions.
2. 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.

Baxter Healthcare Corporation

Reusable blood pressure cuffs labeled "not made with natural rubber latex" when there is a latex-containing rubber band located around the product instructions for use (IFU).

Status : Open

Please review the instructions below and submit your response(s).

To process the return, please follow these steps:

1. Download the recall documentation: FA-2025-007 US Customer Recall 
2. Follow the instructions and contact Baxter Healthcare with next steps (see contact information on Page 2 of linked document)