Recall Z-1098-2022— ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Class I · Terminated
Class I FDA medical device recall by ARJOHUNTLEIGH POLSKA Sp. z.o.o., initiated 2022-04-05, terminated 2024-09-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Sara Plus Active Floor Lift. Reason: The device may emit smoke or ignite..
- Recalling firm
- ARJOHUNTLEIGH POLSKA Sp. z.o.o.
- Classification
- Class I
- Status
- Terminated
- Initiated
- 2022-04-05
- Terminated
- 2024-09-05
- Firm location
- Komorniki, Poland
Product description
Sara Plus Active Floor Lift
Reason for recall
The device may emit smoke or ignite.
Data sourced from openFDA. This site is unofficial and independent of the FDA.