Stryker recalls IsoAir 2.0 support surfaces with potential CPR connector removal issues during cardiac arrest. Affected units have specific serial numbers and model 2941-001-100. Contact Stryker for details.
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
Stryker is recalling certain IsoAir 2.0 support surfaces that may cause delays in CPR during cardiac arrest due to a connector issue. This could be dangerous for patients needing immediate resuscitation.
The connector between the support surface and pump may be out of tolerance, making it difficult to remove the CPR connector. This could delay critical resuscitation efforts during cardiac arrest.
Healthcare providers using the IsoAir 2.0 support surface for cardiac arrest patients are most at risk. Patients in cardiac arrest requiring CPR could experience delays if the recalled unit is used.
Check for model number 2941-001-100 and serial numbers listed in the recall (e.g., 2020018700101 to 2020018700292). The GTIN number is 07613327503999.
Verify if your IsoAir 2.0 support surface has model number 2941-001-100 and one of the listed serial numbers.
Reach out to Stryker directly for further instructions or to confirm if your unit is affected.
The connector between the support surface and pump may be out of tolerance, causing difficulty in removing the CPR connector during cardiac arrest.
Check if your unit has model number 2941-001-100 and one of the listed serial numbers. Contact Stryker for further instructions.
The recall states a potential delay in resuscitation efforts during cardiac arrest, which could be dangerous but does not explicitly state a risk of serious injury.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-3015-2020 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-3015-2020 from Stryker. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
