Product Wiki · Recalls · U.S. FDA — Device Enforcement

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.). — recall Z-2656-2014

U.S. FDA — Device Enforcement · United States · 2014-07-21 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2656-2014
Date of alert: 2014-07-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: GF Health Products, Inc./d.b.a.Basic American Metal Products
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 1169000522

Reported risk: 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.

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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