Reported Apr 22, 2026 · Ongoing

Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US

ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: ARJOHUNTLEIGH POLSKA Sp. z.o.o. · Ul. Ks. Piotra Wawrzyniaka 2 · Komorniki, N/A · N/A

Is this the product you have?

  • Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
Lot codes and dates
  • UDI-DI05055982787758
  • and 05055982787710 Serial Number

    119 of 119 codes

    • P0911221
    • P0909831
    • P0925191
    • P0907166
    • P0901255
    • P0906820
    • P0925431
    • P0912820
    • P0924568
    • P0910471
    • P0903999
    • P0914725
    • P0909539
    • P0910797
    • P0896659
    • P0911350
    • P0925190
    • P0914588
    • P0904321
    • P0905040
    • P0924559
    • P0913229
    • P0909537
    • P0923376
    • P0923377
    • P0911222
    • P0899348
    • P0909201
    • P0900805
    • P0912570
    • P0903592
    • P0912571
    • P0912573
    • P0914003
    • P0900806
    • P0910470
    • P0907737
    • P0907738
    • P0914004
    • P0908250
    • P0908429
    • P0914122
    • P0916220
    • P0912343
    • P0912821
    • P0924239
    • P0925203
    • P0925433
    • P0903476
    • P0912342
    • P0913326
    • P0904320
    • P0905039
    • P0897003
    • P0915180
    • P0898734
    • P0907165
    • P0907736
    • P0897841
    • P0903997
Amount recalled
119 units

Where it was sold

  • Nationwide

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:20 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.