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Terminated

KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL

FDA Recall Z-0522-2014 · Posted 2013-12-17

Recalling Firmmobility unlimited inc
Recall StatusTerminated
Product CodeFNL
Date Initiated2013-04-11
Date Terminated2014-10-08
Product Quantity33 beds

Reason for Recall

Some joints on the doors of a limited number of IDA beds may loosen or separate over time which can cause the doors to drop outward and cause injury.

Firm Action

Mobility Unlimited sent a notification letters dated April 12, 2013 to affected customers The letter identified the affected product, problem and actions to be taken. The letter informed customers that a Retrofit Kits along with illustrated instructions will be sent. For questions call 1-800-574-7880.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - USA Nationwide in the states of AL, AZ, CA, FL, GA, IL, MN, MO, NY, PA, TN, TX, VA, and Canada.

Official Source

View FDA Recall →

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

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