Zenith Slide W-I-D-E Long Term Care Bed — Class II medical device recall Z-2656-2014
Terminated recall by GF Health Products, Inc./d.b.a.Basic American Metal Products, reported 2014-09-24, distributed nationwide. The bed head deck may fail to elevate as expected during normal operation. When the non-operation occurs, the
| Recall number | Z-2656-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GF Health Products, Inc./d.b.a.Basic American Metal Products, Fond Du Lac, WI, United States |
| Recall initiated | 2014-07-21 |
| Classified | 2014-09-16 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2015-08-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,941 |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 26267867430007, 26267867430014, 26267867430021, 26267867430038, 26267867430045, 26267867430052, 26267867430069, 26267867430076, 26267867430083, 26267867430090, 26267867430106, 26267867430113, 26267867430120, 26267867430137, 26267867430144, 26267867430151, 26267867430168, 26267867430175, 26267867430182, 26267867430199, 26267867430205, 26267867430212, 26267867430229, 26267867430236, 26267867430243 and 28 more |
| Serial numbers | 1026904126, 116199810130001, 116199810130110, 116199810130111, 116199810130112, 116199810130113, 116199810130114, 116199810130115, 116199810130116, 116199810130117, 116199810130118, 116199810130119, 116199867411301, 116199867411302, 116199867411303, 116199867411306, 116199867411307, 116199867411308, 116199867411309, 116199867411310, 116199867411311, 116199867411312, 116199867411313, 116199867411314, 116199867411315 and 475 more |
| Model numbers | APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, ZZ98774 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2656-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.