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Terminated

Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.

FDA Recall Z-0105-2019 · Posted None

Recalling FirmLiko AB
Recall StatusTerminated
Product CodeFSA
Date Initiated2018-07-17
Date Terminated2019-04-19
Product Quantity2

Reason for Recall

The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.

Firm Action

The customer was contacted via telephone on 7/17/18 to notify them of the recall. An Urgent Field Safety Notice notification letter was sent to the customer on 7/19/18.

Root Cause

Storage

Distribution Pattern

The products were distributed to the following US states: OH.

Official Source

View FDA Recall →

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

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