Reported Dec 13, 2023 · Ongoing

ProCuity bed series, model number 3009, item number: 3009PX-LE-450.

Stryker Medical Division of Stryker 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: Stryker Medical Division of Stryker Corporation · 3800 E Centre Ave · Portage, MI · 49002-5826

Is this the product you have?

  • ProCuity bed series, model number 3009
  • item number3009PX-LE-450
Lot codes and dates
  • UDI-DI (GTIN)07613327541175
  • Serial numbers
    • 2109000993
    • 2208000147
    • 2209000850
    • 2211002051
    • 2202000910
    • 2209000408
    • 2205000619
    • 2205000615
    • 2205000612
    • 2205000587
    • 2205000746
    • 2205000745
    • 2205000739
    • 2109000135
    • 2109000124

This recall covers 13 products

The agency filed one notice per product. You are reading one of them; the other 12 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.

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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 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.