United StatesWelch Allyn INF BAG, Thigh 1‑Tube replacement bladder for the Welch Allyn two‑piece reusable blood pressure cuff (REF 5089‑18, 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) distributed in California, Colorado, Ohio and Utah (118 units). It was recalled because the replacement bladder kit may contain a Large Adult size bladder rather than a Thigh size bladder.
What's being recalled
Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.
Recalling firm: Baxter Healthcare Corporation, Deerfield, IL, United States.
How to identify it
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
The hazard
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.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide distribution in the states of California, Colorado, Ohio, and Utah.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)