Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0014-2018 — Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009

U.S. FDA — Device Enforcement · Sweden · 2016-07-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0014-2018
Date of alert
2016-07-28
Country / jurisdiction
Sweden
Risk level
Class II
Risk type
recall
Brand
Handicare AB
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
661102000
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.