Recall Z-2656-2014— GF Health Products, Inc./d.b.a.Basic American Metal Products
Class II · Terminated
Class II FDA medical device recall by GF Health Products, Inc./d.b.a.Basic American Metal Products, initiated 2014-07-21, terminated 2015-08-11. FDA's recall record names no specific 510(k) clearance for this event. Product: 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.).. Reason: 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..
- Recalling firm
- GF Health Products, Inc./d.b.a.Basic American Metal Products
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2014-07-21
- Terminated
- 2015-08-11
- Firm location
- Fond Du Lac, WI, United States
Product description
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.).
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.