Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Zenith Slide W-I-D-E Long Term Care Bed Recalled by GF Health Products, Inc./d.b.a.Basic American Metal Products Due to The bed head deck may fail to elevate...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GF Health Products, Inc./d.b.a.Basic American Metal Products directly.
Affected Products
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ98774. Designed for use within an institutional healthcare environment (i.e. assisted living, skilled nursing, transitional care, rehabilitation centers, etc.).
Quantity: 1941
Why Was This Recalled?
The bed head deck may fail to elevate as expected during normal operation. When the non-operation occurs, the head deck remains in the lowered horizontal / flat position and will no longer function as intended.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GF Health Products, Inc./d.b.a.Basic American Metal Products
GF Health Products, Inc./d.b.a.Basic American Metal Products has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report