FDA Medical Device Recalls (openFDA)
Snug Seat Inc: High-low:x frame for the x:panda mechanical chair.
- Recall number
- Z-0651-2009
- Recalling firm
- Snug Seat Inc
- Product
- High-low:x frame for the x:panda mechanical chair.
- Status
- Terminated
- Initiated
- 2008-11-06
- Posted
- 2009-01-05
- Terminated
- 2011-02-17
- Reason
- Breakage in the welds was discovered in a section of the chair frame.
- Root cause
- Process control
- 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.
- Quantity
- 67 units
- Distribution
- Nationwide.
- Lot, serial or model codes
- Article numbers 8911605-02, 8911605-02E, 8911606-02, 8911615-02, 8911615-02E and 8911616-02. Manufactured between 8/24/2007 and 10/3/2008.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IMS
- Firm FEI
- 1053060
- Firm city
- Stallings
- Firm state
- NC
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28