Reported Oct 7, 2020 · Terminated

Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the…

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?

  • Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the microclimate of the patient skin
  • Model Number2941-001-100
Lot codes and dates
  • Serial Numbers

    110 of 110 codes

    • 2020018700101
    • 2020018700102
    • 2020018700103
    • 2020018700104
    • 2020018700105
    • 2020018700106
    • 2020018700107
    • 2020018700108
    • 2020018700109
    • 2020018700110
    • 2020018700111
    • 2020018700112
    • 2020018700113
    • 2020018700114
    • 2020018700115
    • 2020018700116
    • 2020018700117
    • 2020018700118
    • 2020018700119
    • 2020018700120
    • 2020018700121
    • 2020018700122
    • 2020018700123
    • 2020018700124
    • 2020018700125
    • 2020018700126
    • 2020018700127
    • 2020018700128
    • 2020018700129
    • 2020018700130
    • 2020018700131
    • 2020018700132
    • 2020018700133
    • 2020018700134
    • 2020018700135
    • 2020018700136
    • 2020018700137
    • 2020018700138
    • 2020018700139
    • 2020018700140
    • 2020018700141
    • 2020018700142
    • 2020018700143
    • 2020018700144
    • 2020018700145
    • 2020018700146
    • 2020018700147
    • 2020018700148
    • 2020018700149
    • 2020018700150
    • 2020018700151
    • 2020018700152
    • 2020018700153
    • 2020018700154
    • 2020018700155
    • 2020018700156
    • 2020018700157
    • 2020018700158
    • 2020018700159
    • 2020018700160
  • GTIN Number07613327503999
Amount recalled
110 units

Where it was sold

Why it was recalled

Connector between support surface and pump may be out of tolerance resulting in difficulty in removing the CPR connector causing a delay in resuscitation efforts for patients experiencing cardiac arrest and needing CPR

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

Notice updated Apr 2, 2021 · Data as of Sep 19, 6:16 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.