Reported Nov 21, 2018 · Terminated

The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option

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?

  • The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Lot codes and dates
  • Serial Numbers

    2,373 of 2,373 codes

    • 026192
    • 026510
    • 026511
    • 026516
    • 026517
    • 026518
    • 034095
    • 034096
    • 034097
    • 034098
    • 034099
    • 034517
    • 035212
    • 035213
    • 035214
    • 035215
    • 035216
    • 035217
    • 035218
    • 035219
    • 035220
    • 035221
    • 035222
    • 035223
    • 035224
    • 035225
    • 035226
    • 036935
    • 036936
    • 036937
    • 036938
    • 036939
    • 036940
    • 036941
    • 037995
    • 037996
    • 037997
    • 037998
    • 037999
    • 038000
    • 038001
    • 038002
    • 038003
    • 038004
    • 038005
    • 038006
    • 038126
    • 038127
    • 038128
    • 039790
    • 039791
    • 041998
    • 042590
    • 044486
    • 045322
    • 045910
    • 045911
    • 045912
    • 045913
    • 045914
Amount recalled
20,030 total

This recall covers 2 products

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

Where it was sold

Why it was recalled

The beds with the high rail side rail option may not be complaint with IEC 60601-2-52/C1:2010. There is a potential risk of entrapment.

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

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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

Notice updated Apr 28, 2020 · Data as of Sep 19, 6:53 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.