Reported Oct 30, 2024 · Ongoing

smiths medical portex, Y' PIECE 15MM, REF 100/276/000

Smiths Medical ASD Inc.

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: Smiths Medical ASD Inc. · 6000 Nathan Ln N · Minneapolis, MN · 55442-1690

Is this the product you have?

    • smiths medical portex
    • Y' PIECE 15MM
    • REF 100/276/000
Lot codes and dates
  • UDI/DI 35019315011003
  • Lot Numbers
    • 4131841
    • UDI/DI 35019315022405
  • Lot Numbers
    • 4122012
    • 4133227
Amount recalled
9,133 units

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Why it was recalled

Uncertainty in the seal integrity of the sterile packaging.

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

Want the full recall guide?

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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, 7:32 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.