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Terminated

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

FDA Recall Z-0014-2018 · Posted None

Recalling FirmHandicare AB
Recall StatusTerminated
Product CodeFSA
Date Initiated2016-07-28
Date Terminated2018-12-17
Product Quantity9 units

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.

Firm Action

The firm initiated their recall by email on 07/28/2017. The firm directed the consignee to repair the units on site and destroy the affected parts.

Root Cause

Process control

Distribution Pattern

OH, PA, MD

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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