FDA recall, , Moderate risk
ArjoHuntleigh Polska Sp. Z.O.O. Carevo Height-Adjustable Shower Trolley
The Carevo height-adjustable shower trolley can open unintentionally, leading to patient falls and serious injury.
Summary by Recall Canary from the FDA notice
What happened
Arjohuntleigh Polska Sp. z.o.o. of Komorniki, Poland, is voluntarily recalling the Carevo height-adjustable shower trolley, Model Number BAC1111-01, because the side support may open unintentionally when the handles are not fully locked and additional force is applied during patient handling. The FDA added the recall to its Enforcement Report on October 29, 2026.
The recall began on September 25, 2026, and involves 8780 units distributed nationwide in the US. The agency classified the recall on October 29, 2026, and included it in the weekly enforcement report on November 4, 2026.
What to do
The FDA notice gives no instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number matches.
Carevo Height-adjustable shower trolley
- Model number
- BAC1111-01
Recall details
- Posted by FDA
- Recall began
- Status
- Open
- Weekly archive
- Listed the week of Oct 26, 2026
- Sold in
US Nationwide distribution.
- Recalled by
- ARJOHUNTLEIGH POLSKA Sp. z.o.o.Komorniki, Poland
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- FDA event number
- 99900
- Recall number
- Z-0315-2027
- Quantity recalled
- 8780 units
- Recall type
- Voluntary: Firm initiated
All recalls from ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
ARJOHUNTLEIGH POLSKA Sp. z.o.o. began the recall
FDA posted the recall to its Enforcement Report and rated it Class II (moderate risk)
Added to Recall Canary
Summary updated
