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Terminated

Zuma Mobility System Models: Zuma Mobility Assist 412045-01 and Zuma Mobility Trainer 412046-01. Product Usage: Human Non-AC-Powered Patient Lift

FDA Recall Z-1431-2012 · Posted 2012-04-16

Recalling FirmKCI USA, Inc.
Recall StatusTerminated
Product CodeFSA
Date Initiated2012-04-06
Date Terminated2012-06-19
Product Quantity4 units

Reason for Recall

The Zuma Mobility Assist and Trainer have the potential to bind during lowering operation.

Firm Action

KCI sent an Urgent - Voluntary Medical Device Correction notification letters dated April 6, 2012 to all affected customers. The letter identified the affected product, problem and actions to be taken. KCI will contact affected customers to schedule a time to upgrade the device. For questions contact KCL's Customer Technical Service Center at 1-800-275-4524. Select option 3 followed by option 2.

Root Cause

Device Design

Distribution Pattern

USA Nationwide Distribution including the states of ID and FL

Official Source

View FDA Recall →

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

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