Ferno Power X2 Ambulance Cot Recall: Fastening Post May Detach
Ferno recalls Power X2 Ambulance Cots (Model 0015816) due to risk of fastening post detaching. Affected units have specific serial numbers. Stop using immediately if you own one.
Use caution until it’s fixed
The fastening post hardware could loosen allowing the fastening post to detach from the cot
Contact the company
What happened, in plain English
Ferno is recalling Power X2 Ambulance Cots with model number 0015816 because the fastening post hardware could loosen and detach. This poses a risk of the cot becoming unstable during use in ambulances, potentially causing injury. Read more at govinfonow.com/recall/51329-ferno-power-x2-ambulance-cot-recall-fastening-post-may-detach.
Source Summary by GovInfoNow · govinfonow.com/recall/51329-ferno-power-x2-ambulance-cot-recall-fastening-post-may-detach · Updated August 17, 2026 · FDA enforcement record: FDA #Z-0133-2026
Cite this page
“Ferno Power X2 Ambulance Cot Recall: Fastening Post May Detach.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51329-ferno-power-x2-ambulance-cot-recall-fastening-post-may-detach. Based on FDA recall #Z-0133-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0133-2026%22&limit=1).
Why it’s dangerous
The fastening post hardware can loosen over time, causing the post to detach from the cot. This could lead to the cot becoming unstable during transport, potentially causing injury to patients or responders.
Who’s affected
Ambulance crews and emergency responders who use the Ferno Power X2 Ambulance Cot (Model 0015816) are most at risk. The recall affects specific units with listed serial numbers.
How to tell if you have this one
Check if your cot has the model number 0015816 and serial numbers listed in the recall (e.g., 25G036127, 25G036128, etc.). The product is designed for ground transportation ambulances.
- Brand
Ferno- Category
Medical device
What to do — step by step
Check Product Serial Number
Look for the serial numbers listed in the recall (e.g., 25G036127, 25G036128, etc.) on the cot's label.
Stop Using Immediately
If you have a recalled cot, stop using it immediately to prevent potential detachment and instability.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 25 states.
FDA distribution: “US Nationwide distribution in the states of AL, AR, AZ, CA, CO, FL, IS, IL, KY, LA, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, TN, TX, UT, VA, WI, WV.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Florida, Illinois, Kentucky, Louisiana, Minnesota, Missouri, Nebraska, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Utah, Virginia, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 41 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Similar recalls
Latest medical device recalls
Keep exploring
Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0133-2026 (September 11, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0133-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.