Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-3015-2020 — Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the microclimate of the patient skin, Model Number: 2941-001-100

U.S. FDA — Device Enforcement · United States · 2020-08-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-3015-2020
Date of alert
2020-08-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Stryker Medical Division of Stryker Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2020018700101
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.