Tenor is a mobile passive lift — Class II medical device recall Z-2652-2014
Terminated recall by ARJOHUNTLEIGH POLSKA SP. ZO.O., reported 2014-09-24, distributed nationwide. ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader bar) bolt broke during use. There
| Recall number | Z-2652-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | ARJOHUNTLEIGH POLSKA SP. ZO.O., POZNAN, N/A, Poland |
| Recall initiated | 2014-06-10 |
| Classified | 2014-09-16 |
| Reported by FDA | 2014-09-24 |
| Terminated | 2018-06-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BH, CA, DE, ES, FR, GB, IE, IL, IN, IT, MX, NL, NZ, PL, RO, SA, SE, UY, ZA |
| Reason classes | device malfunction |
| Serial numbers | P0111930, P0112213, P0112214, P0117472, P0121496, P0123586, P0125147, P0127106, P0127347, P0127348, P0128923, P0128924, P0129153, P0129154, P0129369, P0129370, P0131041, P0131526, P0131527, P0131773, P0131774, P0133024, P0134145, P0134146, P0136335 and 357 more |
| Model numbers | KHA1000-US |
Product
Tenor is a mobile passive lift, intended to be used on horizontal surfaces for lifting and transfer in hospitals, nursing homes or other healthcare facilities. Transfers with the Tenor are made indoors in the patient's room, in communal areas or in a bathroom. Tenor is meant to be used with the patient type who: sits in a wheelchair, has no capability to support themselves at all, cannot stand unsupported and is not able to bear weight (not even partially), is dependent on caregiver in most situations, is a passive resident, might be almost completely bed ridden, is often stiff and has contracted joints, and/or is totally dependent. The Tenor has a safe working load of 320 KG (705 lbs).
Reason for recall
ArjoHuntleigh received reports where the Tenor Lift without Scale (spreader bar) bolt broke during use. There is a remote risk concerning the breakage of the spreader bar bolt connection, part # TEN.018. During use, the bolt is subjected to mechanical forces, which may lead to breakage.
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-2652-2014. 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.