ARJOHUNTLEIGH POLSKA Sp. z.o.o.
5 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US recall (Z-1811-2026) | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | 2026-04-10 |
| Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel recall (Z-0611-2024) | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | 2023-12-22 |
| Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel recall (Z-0612-2024) | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | 2023-12-22 |
| Sara Plus Active Floor Lift recall (Z-1098-2022) | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | 2022-05-21 |
| Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting recall (Z-2693-2014) | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | 2014-09-24 |
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Every clearance here is in the API, with alerts when new ones post.