FDA Device recall Z-1098-2022
Sara Plus Active Floor Lift
- FDA Device
- Class I
- terminated
- Published 2022-06-01
On 2022-06-01 the FDA classified a Class I recall of Sara Plus Active Floor Lift by Arjohuntleigh Polska Sp Z O O, citing the device may emit smoke or ignite.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1098-2022 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2022-04-05 |
| Published | 2022-06-01 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Arjohuntleigh Polska Sp Z O O |
| Distribution | US |
Product
Sara Plus Active Floor Lift
Reason
The device may emit smoke or ignite.
Identifiers
| code_info | Model Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, H…Model Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Other recalls by Arjohuntleigh Polska Sp Z O O
- Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
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FDA Device · Class II · 2024-01-03 · Arjohuntleigh Polska Sp Z O O - Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module a…
FDA Device · Class II · 2024-01-03 · Arjohuntleigh Polska Sp Z O O - Arjo Citadel beds originally assembled with the IndiGo modules during manufcturing, model number CX812A3J3AMAD0
FDA Device · Class II · 2021-10-06 · Arjohuntleigh Polska Sp Z O O - Bariatric Bed Frame System The Citadel Plus Bariatric Bed Frame System is intended for the acute and post-acute care environments
FDA Device · Class II · 2020-08-26 · Arjohuntleigh Polska Sp Z O O
All Arjohuntleigh Polska Sp Z O O recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1098-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.