FDA Device recall Z-0079-2015
Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift
- FDA Device
- Class II
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class II recall of Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift by Arjo, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0079-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-01-21 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arjo |
| Distribution | AR, DC, GA, MI, PA |
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
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.
Identifiers
| code_info | Serial numbers 1942500017, 1942500025, 1942500030, 1942500053, 1942500054, 1942500055, 1942500056, 1942500057, 19425000…Serial numbers 1942500017, 1942500025, 1942500030, 1942500053, 1942500054, 1942500055, 1942500056, 1942500057, 1942500058, 1942500059, 1942500060, 1942500061, 1942500062, 1942500063, 1942500064, 1942500065, 1942500066, 1942500067, 1942500068, 1942500069, 1942500070, 1942500071, 1942500072, 1942500073, 1942500074, 1942500075, 1942500076, 1942500077, 1942500078, 1942500079, 1942500080, 1942500081, 1942500082, 1942500083, 1942500085, 1942500086, 1942500087, 1942500088, 1942500089, 1942500092, 1942500093, 1942500094, 1942500095, 1942500096, 1942500097, 1942500098, 1942500099, 1942500100, 1942500101, 1942500102, 1942500103, 1942500104, 1942500105, 1942500106, 1942500107, 1942500108, 1942500109, 1942500110, 1942500111, 1942500112, 1942500113, 1942500114, 1942500115, 1942500116, 1942500117, 1942500118, 1942500119, 1942500120, 1942500121, 1942500122, 1942500123, 1942500124, 1942500125, 1942500126, 1942500127, 1942500128, 1942500129, 1942500130, 1942500131, 1942500132, 1942500133, 19425 |
|---|
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-0079-2015%22
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