510(k) · Cleared
Recalled · 2003EZ Load Model 30, All Level Cot
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ferno-Washington, Inc. · FPO Stretcher, Wheeled
Cleared on Sep 12, 1986 after a 78-day review. FDA has not posted a summary or statement for it, so its predicates are not known. It has been recalled 2 times.
- Decided
- Sep 12, 1986
- Review
- 78 days
- Class
- Class II
- Product code
- FPO
- Recalls
- 2
- Predicates
- 0
FDA has not posted a summary or statement for it, so its predicates are not known.
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FPO? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Mar 28, 2003 | Not classified | Z-0202-06 | Other | The firm received complaints of the stretchers folding. A fold is when the stretcher lowers on its own to either the next position, or any of the other seven postions of the stretcher. |
| Mar 28, 2003 | Not classified | Z-0201-06 | Other | The firm received complaints of the stretchers folding. A fold is when the stretcher lowers on its own to either the next position, or any of the other seven postions of the stretcher. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All FPO devicesFPO Stretcher, Wheeled: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FPO
1in 2011
2026 to Oct 25, outlined.
Median 510(k) review, days · FPO
Too few FPO 510(k)s in any year since 2007 to give a median.
Recalls per year · FPO
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FPO
897in 2025
MAUDE reports naming product code FPO, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 6 | 117 |
| 2008 | 1 | — | 3 | 385 |
| 2009 | 0 | — | 12 | 2,337 |
| 2010 | 0 | — | 1 | 4,049 |
| 2011 | 1 | — | 6 | 5,891 |
| 2012 | 0 | — | 1 | 6,334 |
| 2013 | 0 | — | 0 | 5,743 |
| 2014 | 0 | — | 1 | 1,633 |
| 2015 | 0 | — | 0 | 381 |
| 2016 | 0 | — | 1 | 205 |
| 2017 | 0 | — | 0 | 230 |
| 2018 | 0 | — | 0 | 573 |
| 2019 | 0 | — | 0 | 663 |
| 2020 | 0 | — | 0 | 694 |
| 2021 | 0 | — | 0 | 874 |
| 2022 | 0 | — | 2 | 694 |
| 2023 | 0 | — | 0 | 1,028 |
| 2024 | 0 | — | 0 | 956 |
| 2025 | 0 | — | 1 | 897 |
| 2026 | 0 | — | 2 | — |
https://510kreport.com/device/K862441 · printed Nov 5, 2026
Cite this page
510(k) Report. “K862441: EZ Load Model 30, All Level Cot.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K862441
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026