Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling…
Medical device recall Z-0079-2015. Published in FDA’s Enforcement Report on Oct 22, 2014.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Oct 22, 2014. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- 5 states named in where it went
- 363 spreader bars how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are 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.
363 spreader bars, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Serial numbers 1942500017, 1942500025, 1942500030, 1942500053, 1942500054, 1942500055, 1942500056, 1942500057, 1942500058, 1942500059, 1942500060, 1942500061, 1942500062, 1942500063, 1942500064, 1942500065, 1942500066, 1942500067,…
Every code shown here, 1,999 characters
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, 1942500134, 1942500135, 1942500136, 1942500137, 1942500138, 1942500139, 1942500140, 1942500141, 1942500142, 1942500143, 1942500144, 1942500145, 1942500146, 1942500147, 1942500148, 1942500149, 1942500150, 1942500151, 1942500152, 1942500153, 1942500154, 1942500155, 1942500156, 1942500157, 1942500158, 1942500159, 1942500160, 1942500161, 1942500162, 1942500163, 1942500164, 1942500165, 1942500166, 1942500167, 1942500168, 1942500169, 1942500170, 1942500171, 1942500172, 1942500173, 1942500174, 1942500175, 1942500176, 1942500177, 1942500178 1942500179 1942500180 1942500181 1942500182 1942500183 1942500185 1942500186 1942500187 1942500188 1942500189 1942500190 1942500191 1942500192 1942500193 1942500194 1942500195 1942500196 1942500197 1942500198 1942500199 1942500200 1942500201 1942500202 1942500203 1942500204 1942500205 1942500206 1942500207 1942500208 1942500210 1942500211 1942500212 1942500213 1942500214 1942500215 1942500216 1942500217 1942500218 1942500219 1942500221 1942500222 1942500223 1942500224…
FDA’s list runs to 3,841 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
USA Distribution - AR, GA, MI, PA, and the District of Columbia.
The states and territories these words name
- Arkansas
- District of Columbia
- Georgia
- Michigan
- Pennsylvania
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Jan 21, 2013.
- FDA classified it on Oct 16, 2014.
- FDA’s Enforcement Report published it on Oct 22, 2014.
- FDA terminated it on Oct 27, 2015.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Arjo, Inc. dba ArjoHuntleigh, of Addison, IL.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 3,841 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.