Reported Apr 23, 2025 · Ongoing
Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits labeled as: 1. WELCH ALLYN 2-Piece Reusable Blood Pressure Cuff…
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 2-Piece Reusable
- Blood Pressure Cuff Kits labeled as1. WELCH ALLYN 2-Piece Reusable Blood Pressure Cuff Kits
- Product Code/Part Numbers2. WELCH ALLYN Reusable Blood Pressure Cuff Kit
- Product Code/Part Numbers
4105195090-415098-20
- Lot codes and dates
35 of 35 products
Products covered by this recall Model / number Barcodes Product as published 47-15-38900732094002423Product Code/ , UDI/DI 00732094002423 47-22-18900732094002379Product Code/ , UDI/DI 00732094002379 47-23-18900732094002362Product Code/ , UDI/DI 00732094002362 5082-0100732094113723Product Code/ , UDI/DI 00732094113723 5082-01H00732094113693Product Code/ , UDI/DI 00732094113693 5082-0200732094113679Product Code/ , UDI/DI 00732094113679 5082-0300732094113648Product Code/ , UDI/DI 00732094113648 5082-0700732094113631Product Code/ , UDI/DI 00732094113631 5082-0800732094113600Product Code/ , UDI/DI 00732094113600 5082-1100732094113327Product Code/ , UDI/DI 00732094113327 5082-1600732094113105Product Code/ , UDI/DI 00732094113105 5082-2100732094112344Product Code/ , UDI/DI 00732094112344 5082-2200732094112290Product Code/ , UDI/DI 00732094112290 5082-22H00732094112276Product Code/ , UDI/DI 00732094112276 5082-2300732094112245Product Code/ , UDI/DI 00732094112245 5082-23H00732094112221Product Code/ , UDI/DI 00732094112221 5082-2400732094112207Product Code/ , UDI/DI 00732094112207 5082-2500732094111996Product Code/ , UDI/DI 00732094111996 5082-2600732094111897Product Code/ , UDI/DI 00732094111897 5082-4200732094111873Product Code/ , UDI/DI 00732094111873 - Amount recalled
- 76407 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Why it was recalled
Undeclared natural rubber band within the packaging of certain configurations of reusable blood pressure cuffs.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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