Arjo, Inc. Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4ELU2FUS Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4ELU2FUS
Brand
Arjo, Inc.
Lot Codes / Batch Numbers
Model number KMMB4ELU2FUS, serial numbers SEE0624509, SEE0624510, SEE0624511, SEE0624512, SEE0624513, SEE0624514, located underneath the removable battery. Serial numbers are all structured SEEYYWWXXX, where ¿ YY = the last two digits of the year, ¿ WW = the two digits of the production week, it is affected by this notification, regardless of the last three digits of the serial number.)
Products Sold
Model number KMMB4ELU2FUS, serial numbers SEE0624509, SEE0624510, SEE0624511, SEE0624512, SEE0624513, SEE0624514, SEE0624515 (Manufactured week 24 of 2006 through week 28 of 2006. You can check the model and serial number of your unit by looking at the serial number label on the mast of the lift, located underneath the removable battery. Serial numbers are all structured SEEYYWWXXX, where ¿ YY = the last two digits of the year, ¿ WW = the two digits of the production week, and ¿ XXX = the sequential number the unit was in production that week ¿ Example: SEE06024001 = the first unit produced in week 24 of 2006. If your equipment has one of the model numbers listed above and a serial number beginning with SEE0624 through SEE0628, it is affected by this notification, regardless of the last three digits of the serial number.)
Arjo, Inc. is recalling Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model due to The hanger bar assembly may detach from the Maxi Move lifters with scale, due to an incorrect torque setting on the two bolts holding the scale in pla. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The hanger bar assembly may detach from the Maxi Move lifters with scale, due to an incorrect torque setting on the two bolts holding the scale in place.
Recommended Action
Per FDA guidance
Arjo sent Urgent Device Field Correction Recall Notice letters dated 1/5/07 to the end user accounts who received the affected lifts, advising them of the potential for the hanger bar assembly to detach. They were informed that an Arjo Field Service Technician would call them within five business days to schedule the time for him to visit and perform the inspection and correction to the lifts involved. If they did not hear from the technician within that time, they were instructed to contact the Arjo Quality Department at 800-323-1245, ext. 6140. The accounts were also requested to complete and return the enclosed customer response form, acknowledging the receipt and understanding of the letter.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026