Arjo Tenor mobile passive patient lift — Class II medical device recall Z-1811-2026
Ongoing recall by ARJOHUNTLEIGH POLSKA Sp. z.o.o., reported 2026-04-22, distributed nationwide. An internal component of the actuators in a certain production batch may not meet the required mechanical stre
| Recall number | Z-1811-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o., Komorniki, N/A, Poland |
| Recall initiated | 2026-03-10 |
| Classified | 2026-04-10 |
| Reported by FDA | 2026-04-22 |
| Distributed | Nationwide (US) |
| Quantity | 119 units |
| Reason classes | potency |
| UPC / GTIN / UDI-DI | 05055982787710, 05055982787758 |
| Serial numbers | P0896658, P0896659, P0897002, P0897003, P0897247, P0897248, P0897841, P0897842, P0898734, P0898735, P0899214, P0899215, P0899348, P0899349, P0900415, P0900805, P0900806, P0901254, P0901255, P0903476, P0903477, P0903591, P0903592, P0903997, P0903998 and 94 more |
| Model numbers | KHA1000US, KHA1010US |
Product
Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Reason for recall
An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the load, leading to rapid and uncontrolled downward movement of the lifting arm.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1811-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.