Stryker recalls 2860 IsoFlex LAL Support Surfaces with non-conforming fire barrier. These medical devices for pressure injury prevention may pose fire risk if improperly used in healthcare settings.
Certain 2860 IsoFlex LAL support surfaces were assembled with a non-conforming fire barrier.
Stryker is recalling certain IsoFlex LAL Support Surfaces (Model 2860) that were assembled with a non-conforming fire barrier. This defect could potentially cause fire risk in healthcare settings where the product is used.
The recalled units have a fire barrier that doesn't meet safety standards. In healthcare environments where patients are at risk of pressure injuries, this defect could lead to fire hazards if the product is used without proper fire safety measures.
Healthcare professionals using the IsoFlex LAL Support Surface in acute care settings with patients at risk of pressure injuries. Patients must be at least two years old and the product should only be used with a support surface cover.
Check for the model number 2860 on the product. The serial numbers listed in the recall include many 2018032860190005xx patterns. These units were sold in acute care settings for patients with pressure injury risks.
Look for the serial numbers listed in the recall (e.g., 201803286019000540) on the product.
If you have a recalled unit, contact Stryker directly for a replacement or repair.
The recalled product is the IsoFlex LAL Support Surface, Model Number 2860.
The recalled units were assembled with a non-conforming fire barrier that does not meet safety standards.
Healthcare professionals in acute care settings using the product with patients at risk of pressure injuries who are at least two years old.
Check the serial number against the list of numbers provided in the recall notice (e.g., 201803286019000540).
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-3181-2018 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-3181-2018 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.
