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Terminated

Bath Safe Adjustable Shower Seat, With Arms, Model numbers 727142020, 727142021, and MDS89750R

FDA Recall Z-0460-2010 · Posted 2009-12-01

Recalling FirmNutech Manufacturing Corp
Recall StatusTerminated
Product CodeIKX
Date Initiated2009-07-09
Date Terminated2013-05-29
Product Quantity3,627 total units

Reason for Recall

Safety chair used in shower/bath may not meet specifications for weight load.

Firm Action

The subsidiary distributor, Maddak, Inc. notified customers by A "Voluntary Product Recall Notice", phone and e-mail on 07/09/2009. The own label distributor instructed customers to return their inventory of affected products received between May 1, 2009 and July 7, 2009. Distributors were instructed to immediately quarantine then return all affected inventory to Maddak and notify their accounts. Distributors were requested to instruct dealers to display a "storefront" notice and provide consumers with a customer response form. Distributors were also requested to forward a request to dealers to post a website notice if they have one. Recovered products will be replaced.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution -- USA and Canada.

Official Source

View FDA Recall →

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

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