Reported Apr 13, 2022 · Ongoing

Lum Lam Custom Pack - Anesthesia Kit

Stradis Medical, LLC dba Stradis Healthcare

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: Stradis Medical, LLC dba Stradis Healthcare · 3025 Northwoods Pkwy · Peachtree Corners, GA · 30071-1524

Is this the product you have?

  • Lum Lam Custom Pack - Anesthesia Kit
Lot codes and dates
  • SKU/Part Number 570-2674
  • UDI H65257026741 Lot Numbers21300478831 and 21314479685
Amount recalled
21 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

Why it was recalled

The outer bag may be perforated or torn, which may result in a breach in the sterility of the kit.

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, 5:35 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.