Handicare AB: Medical Device Recall in 2017 - (Recall #: Z-0014-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

Product Classification:

Class II

Date Initiated: July 28, 2016

Date Posted: October 18, 2017

Recall Number: Z-0014-2018

Event ID: 78130

Reason for Recall:

A limited amount of Carina mobile lifts have been delivered with a too small locking pin. If a locking pin smaller than the correct size is mounted on the Carina mobile lift, the locking pin is likely to cause increased wear on the plastic bushings. In case of continued use, these components may cause wear on the metal of the piston rod eye.

Status: Terminated

Product Quantity: 9 units

Code Information:

a) Carina350EM, REF 6060011, Serial numbers: 661102000 - 661102160 b) Carina350EML, REF 60600012, Serial numbers: 661200500 - 661200584 c) Carina350EE, REF 60600009, Serial numbers: 660900500 -660900571

Distribution Pattern:

OH, PA, MD

Voluntary or Mandated:

Voluntary: Firm initiated