Arjohuntleigh Polska Sp. Z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland: Lift, Patient, Non-ac-powered
- Recalling firm
- ARJOHUNTLEIGH POLSKA Sp. z.o.o. Ul. Ks. Piotra Wawrzyniaka 2 Komorniki Poland
- Product
- Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
- Reason
- An internal component of the actuators in a certain production batch may not meet the required mechanical strength. This could result, in the worst case scenario, in a sudden loss of the actuator's ability to hold the load, leading to rapid and uncontrolled downward movement of the lifting arm.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-03-10
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b9bed854-b3c8-470e-8eb8-433cc77fd411