Reported Dec 10, 2025 · Ongoing

Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn…

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Welch Allyn INF BAG, Thigh 1-Tube
  • Model/Catalog NumberREF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff
Lot codes and dates
  • UDI- DI 00732094110845
  • Lot Numbers
    • 23-296
    • 23-318
    • 23-325
    • 23-353
    • 24-008
    • 24-036
    • 24-037
    • 24-138
    • 24-183
    • 25-037
    • 25-112
    • 25-119
    • 25-180
Amount recalled
118 units

Where it was sold

Why it was recalled

Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 4:15 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.