ARJOHUNTLEIGH POLSKA Sp. z.o.o.
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
1 category · 2026-04-22 to 2026-04-22
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-04-22 | FDA Device | FDA Recall: Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US | ARJOHUNTLEIGH POLSKA Sp. z.o.o. | Class II | N/A |