Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported October 22, 2014
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.
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 positione…
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Arjo, Inc. dba ArjoHuntleigh recalled Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on th… - a moderate-severity action.
Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on th… was recalled by Arjo, Inc. dba ArjoHuntleigh in October 22, 2014. Reason: The upper portion of the hooks on the spreader bar are too flexible for holding the loops of the sling. The …. Check the official notice for the remedy. Verify recall #Z-0079-2015 with the FDA Devices before acting.
The recall
Arjo, Inc. dba ArjoHuntleigh issued this moderate-severity FDA Devices recall-The upper portion of the hooks on the spreader bar are too flexible for holding the loops of the sling. The ….
- Moderate
- severity level
- Class II
- classification
- October 22, 2014
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-0079-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-0079-2015) was formally reported on October 22, 2014, with the manufacturer initiating the action on January 21, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Arjo, Inc. dba ArjoHuntleigh is listed as the recalling firm, operating out of Addison, IL. Federal records list the affected scope as 363 spreader bars.
The documented reason for this recall is: 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. Distribution data in the federal record shows the product reached: USA Distribution - AR, GA, MI, PA, and the District of Columbia.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
363 spreader bars
Related Recalls
6
3 from same agency
Product description
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-0079-2015 |
| Date reported | October 22, 2014 |
| Date initiated | January 21, 2013 |
| Recalling firm | Arjo, Inc. dba ArjoHuntleigh |
| Firm location | Addison, IL |
| Affected scope | 363 spreader bars |
| Distribution | USA Distribution - AR, GA, MI, PA, and the District of Columbia. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-0079-2015) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
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.. Recalled by Arjo, Inc. dba ArjoHuntleigh. Units affected: 363 spreader bars.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 22, 2014. Severity: Moderate. Recall number: Z-0079-2015.
Where was the recalled product distributed? ▼
Distribution: USA Distribution - AR, GA, MI, PA, and the District of Columbia..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-0079-2015) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported October 22, 2014. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.