Data Foundry

Medical device recalls 2014

Medium 2-Hooks Spreader Bar for use with Loop Slings — Class II medical device recall Z-0079-2015

Terminated recall by Arjo, Inc. dba ArjoHuntleigh, reported 2014-10-22, distributed in AR, DC, GA, MI, PA. The upper portion of the hooks on the spreader bar are too flexible for holding the loops of the sling. The lo

Recall numberZ-0079-2015
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmArjo, Inc. dba ArjoHuntleigh, Addison, IL, United States
Recall initiated2013-01-21
Classified2014-10-16
Reported by FDA2014-10-22
Terminated2015-10-27
DistributedAR, DC, GA, MI, PA
Quantity363 spreader
Serial numbers1942500017, 1942500025, 1942500030, 1942500053, 1942500054, 1942500055, 1942500056, 1942500057, 1942500058, 1942500059, 1942500060, 1942500061, 1942500062, 1942500063, 1942500064, 1942500065, 1942500066, 1942500067, 1942500068, 1942500069, 1942500070, 1942500071, 1942500072, 1942500073, 1942500074 and 311 more
Model numbers700-19425

Product

Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Model 700-19425. Intended to be used for general transfers in hospitals.

Reason for recall

The upper portion of the hooks on the spreader bar are too flexible for holding the loops of the sling. The loop of the sling could potentially come out of the hooks if positioned in the upper portion of the hooks.

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-0079-2015. 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.