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Terminated

High-low:x frame for the x:panda mechanical chair.

FDA Recall Z-0651-2009 · Posted 2009-01-05

Recalling FirmSnug Seat Inc
Recall StatusTerminated
Product CodeIMS
Date Initiated2008-11-06
Date Terminated2011-02-17
Product Quantity67 units

Reason for Recall

Breakage in the welds was discovered in a section of the chair frame.

Firm Action

Consignees were notified by letter dated 11/6/2008. Snug Seat sent a repair kit to their retail dealers on 11/18/2008. The kit includes a safety plate, written and video replacement instructions as well as the tools (allen wrench, crescent wrench and two nuts) necessary to make the safety update. Customers were identified using purchase order numbers, and product serial numbers to enable the dealers to identify the purchaser of the product. Due to HIPPA regulations, purchaser information was not available to Snug Seat, Inc. to contact directly. Written notification will be followed up with a telephone call to each dealer to ensure they have received the retrofit kit. Snug Seat will also insure they understand the importance of the kit and how to properly install and document receipt of the update for their customers.

Root Cause

Process control

Distribution Pattern

Nationwide.

Official Source

View FDA Recall →

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

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