FDA Device recall Z-2656-2014
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ987…
- FDA Device
- Class II
- terminated
- Published 2014-09-24
On 2014-09-24 the FDA classified a Class II recall of Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ987… by Gf Health Products D B A Basic American Metal Products, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2656-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-21 |
| Published | 2014-09-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Gf Health Products D B A Basic American Metal Products |
| Distribution | US |
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.
Identifiers
| code_info | Model # Serial # APS98674 1161998674140123 APS98674 1169000522 APS98674 1161998674130104 APS98674 1161998674130105…Model # Serial # APS98674 1161998674140123 APS98674 1169000522 APS98674 1161998674130104 APS98674 1161998674130105 APS98674 1169000642 APS98674 1169000643 APS98674 1161998674130049 APS98674 1161998674130002 APS98674 1161998674130003 APS98674 1161998674130004 APS98674 1161998674130005 APS98674 1161998674130006 APS98674 1161998674130007 APS98674 1161998674130008 APS98674 1161998674130009 APS98674 1161998674130010 APS98674 1161998674130011 APS98674 1161998674130012 APS98674 1161998674130013 APS98674 1161998674130014 APS98674 1161998674130015 APS98674 1161998674130016 APS98674 1161998674130017 APS98674 1161998674130018 APS98674 1161998674130019 APS98674 1161998674130020 APS98674 1161998674130021 APS98674 1161998674130022 APS98674 1161998674130023 APS98674 1161998674130024 APS98674 1161998674130025 APS98674 1161998674130026 APS98674 1161998674130027 APS98674 1161998674130028 APS98674 1161998674130029 APS98674 1161998674130030 APS98674 1161998674130031 A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2656-2014%22
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