Z-0797-2007

Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model...

Name: Z-0797-2007 Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model...
Creator: Arjo, Inc.
Published: 2007-01-05
License: https://open.fda.gov/license/

Arjo, Inc. / initiated 2007-01-05 / Terminated

FDA source

Arjo, Inc. began a recall of Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4MSU2FUS on 2007-01-05. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0797-2007
Status: Terminated
Initiated: 2007-01-05
Posted: 2007-05-11
Terminated: 2008-09-02
Recalling firm: Arjo, Inc.
Product: Maxi Move Patient Lift with Scale; Manufactured by Arjo Hospital Equipment AB, Eslov, Sweden; Model KMBB4MSU2FUS
Product code: FSG
Reason for recall: 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.
FDA root cause: Other
Action: 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.
Quantity in commerce: 10 lifts
Distribution: Nationwide
Product codes and lots: Model number KMBB4MSU2FUS, serial numbers SEE0628311, SEE0628312, SEE0628314, SEE0628315, SEE0628319, SEE0628320, SEE0628322, SEE0628323, SEE0628324, SEE0628326 (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.)

Product code FSG

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)