Chorus Mobile Patient Lifter — Class II medical device recall Z-1948-2012
Terminated recall by Arjo, Inc. dba ArjoHuntleigh, reported 2012-07-18, distributed nationwide. ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed meta
| Recall number | Z-1948-2012 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Arjo, Inc. dba ArjoHuntleigh, Addison, IL, United States |
| Recall initiated | 2012-06-29 |
| Classified | 2012-07-06 |
| Reported by FDA | 2012-07-18 |
| Terminated | 2018-03-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, BM, CA, CH, CY, CZ, DE, DK, EE, ES, FI, FR, GB, GR, HK, IE, IL, IS, IT, JP, KE, KR, LU, NL, NO, NZ, PL, PT, SA, SE, SG, SI, SK, TR |
| UPC / GTIN / UDI-DI | 00010390930405, 00050186430610, 00050288913707, 00050391134808, 00050391134907, 00060391201103, 00060391201110, 00060391261107, 00080289003503, 00080289003510, 00090186431002, 00090391293402, 00090391328807, 00100186431107, 00100289064103, 00100289064110, 00110289188501, 00110391375202, 00110391404209, 00120186815004, 00140186815101, 00140186820204, 00140186820303, 00150186994003, 00150289328101 and 130 more |
| Serial numbers | 010390930401, 010390930403, 010390930404, 010390930405, 010390930406, 010390930407, 010390930408, 010390930409, 010390930410, 010391015510, 020493522101, 020493522102, 020493522103, 020493522104, 020493522105, 020493522106, 030391005101, 030391048708, 030391048709, 040391133401, 040391133402, 040391133403, 040391133404, 040391133408, 040391133409 and 475 more |
| Model numbers | KKB5060-21US, KKB5062-21US, KKB5080-21US |
Product
Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position to another, and to elevate a patient for toileting, repositioning, changing of incontinence pads or wound dressings, standing practice etc. it is not intended for long periods of suspension or transportation.
Reason for recall
ArjoHuntleigh has received a limited number of customer reports concerning injuries related to an exposed metal support bracket when the proactive knee pad assembly is removed.
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-1948-2012. 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.