Use cautionMedical device recall · FDA · Published August 12, 2020
Stryker IsoAir 2.0 Support Surface Recall: CPR Connector May Cause Delay in Resuscitation
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
Take action
Contact the company
📍Recalling firmStryker Medical Division of Stryker Corporation3800 E Centre Ave · Portage, MI 49002-5826
“Stryker IsoAir 2.0 Support Surface Recall: CPR Connector May Cause Delay in Resuscitation.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64494-stryker-isoair-2-0-support-surface-recall-cpr-connector-may. Based on FDA recall #Z-3015-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3015-2020%22&limit=1).
The FDA announced on Aug. 12, 2020, that Stryker Medical Division of Stryker Corporation is voluntarily recalling the IsoAir 2.0 support surface due to a connector tolerance issue. The defect may cause difficulty removing the CPR connector, potentially delaying resuscitation efforts for patients in cardiac arrest.
How to tell if you have it
Brand: Stryker
Product: IsoAir 2.0 support surface
Model Number: 2941-001-100
UPC/GTIN: 07613327503999
Units affected: 110
Sold: Nationwide in the US, including CA, FL, NY, OH
The hazard
The connector between the support surface and pump may be out of tolerance. This defect can result in difficulty removing the CPR connector, causing a delay in resuscitation efforts for patients experiencing cardiac arrest who need CPR.
Context
GovInfoNow's records show Stryker Medical Division of Stryker Corporation has had 17 other recalls on record since July 21, 2017. Recent recalls include the Feb. 18, 2026, recall of Cub Pediatric Cribs for missing warning labels and the Oct. 31, 2025, recall of MV3 Bariatric Beds regarding mattress compatibility. Other recent recalls of similar products include the Stryker XCEL Bladeless Trocar W/Stability Sleeve 5x75mm Recall (Aug. 19, 2026) and the Stryker CS Uni-Directional w Auto ID Catheter Recall (April 10, 2026).
How to tell if you have this one
Check for model number 2941-001-100 and serial numbers listed in the recall (e.g., 2020018700101 to 2020018700292). The GTIN number is 07613327503999.
Brand
Stryker
Product
Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check for Recalled Unit
Verify if your IsoAir 2.0 support surface has model number 2941-001-100 and one of the listed serial numbers.
Contact Stryker
Reach out to Stryker directly for further instructions or to confirm if your unit is affected.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution including in the states of CA, FL, NY, OH.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Florida, New York, Ohio.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-3015-2020 (August 12, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3015-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.