ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls
Every recall we track for ARJOHUNTLEIGH POLSKA Sp. z.o.o. — 8 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them. 2 are rated “stop using now”.
Recalls per year, by danger level
8 recalls since 2017. 25% rated “stop using now”.
All FDA recall records for ARJOHUNTLEIGH POLSKA Sp. z.o.o. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 1 | 0 | 0 | 0 | 1 |
| 2019 | 0 | 1 | 0 | 0 | 1 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 0 | 0 | 1 |
| 2023 | 0 | 2 | 0 | 0 | 2 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls
What to do if you have a recalled ARJOHUNTLEIGH POLSKA Sp. z.o.o. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls
7 shown- Use cautionMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Recall of Arjo Tenor mobile passive patient lifts (models KHA1000 US and KHA1010 US) due to potential actuator failure causing uncontrolled drop. Affected units have specific serial numbers.
ArjoMar 10, 2026 - Use cautionMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive
Arjo recalls Enterprise 5000X, 8000X, 9000X and Citadel medical beds with IndiGo Drive modules due to unintended wheel movement. Affected units have specific serial numbers and UDI/DI codes.
ArjoAug 29, 2023 - Stop using nowMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Sara Plus Active Floor Lift
ARJOHUNTLEIGH POLSKA recalls Sara Plus Active Floor Lift models due to potential fire risk from smoke emission. Affected units include HEP0001 series and HEP2001 variants sold globally. Consumers should stop using immediately.
ARJOHUNTLEIGH POLSKAApr 5, 2022 - Lower riskMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0; and
Arjo Citadel beds made between May 2018 and February 2021 with IndiGo modules may have power cords that wear, potentially causing cuts, burns, or short circuits. Affected units include specific model numbers and retrofitted kits.
ArjoJun 10, 2021 - Lower riskMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care
ARJOHUNTLEIGH POLSKA recalls bariatric bed frames with modular junction box cables that may melt, affecting functionality. Serial numbers P0597830 to P0610470 are affected.
ARJOHUNTLEIGH POLSKAJul 21, 2020 - Use cautionMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Concerto & Basic Shower Trolly, Model Numbers BAB1000-01 (UDI: (01)05055982788083), BAB1000CON6102
ARJOHUNTLEIGH POLSKA recalls Concerto and Basic Shower Trolly models with potential safety catch failure that could cause patient falls. Affected units include specific model numbers and serial ranges. No remedy is stated in the recall notice.
ARJOHUNTLEIGH POLSKAAug 22, 2019 - Stop using nowMedical device
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo Passive Clip Sling is a product
Arjo recalls passive clip slings that may break during patient transfers, risking falls and serious injury. Affected units have specific model and lot numbers.
ArjoOct 22, 2018
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall questions
How many recalls has ARJOHUNTLEIGH POLSKA Sp. z.o.o. had?
8 recalls from ARJOHUNTLEIGH POLSKA Sp. z.o.o. are on record with U.S. safety agencies, from 2018–2026.
What is the most recent ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall?
ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US, dated Mar 10, 2026. Every ARJOHUNTLEIGH POLSKA Sp. z.o.o. recall is listed on this page, newest first.
Why are ARJOHUNTLEIGH POLSKA Sp. z.o.o. products recalled?
The most common reasons on record: Unintended movement of bed wheels (2).
What should I do if I have a recalled ARJOHUNTLEIGH POLSKA Sp. z.o.o. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new ARJOHUNTLEIGH POLSKA Sp. z.o.o. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.