FDA Medical Device Recalls (openFDA)
Nutech Manufacturing Corp: Shower Seat, Non-rotating, Catalog number 727152000
- Recall number
- Z-0464-2010
- Recalling firm
- Nutech Manufacturing Corp
- Product
- Shower Seat, Non-rotating, Catalog number 727152000
- Status
- Terminated
- Initiated
- 2009-07-09
- Posted
- 2009-12-01
- Terminated
- 2013-05-29
- Reason
- Safety chair used in shower/bath may not meet specifications for weight load.
- Root cause
- Device Design
- 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.
- Quantity
- 3,627 total units
- Distribution
- Worldwide Distribution -- USA and Canada.
- Lot, serial or model codes
- Device is not identified with a lot code. Inventories received between May 1, 2009 and July 7, 2009 are being recalled.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- IKX
- Firm FEI
- 3006525314
- Firm city
- Pocomoke City
- Firm state
- MD
- 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