FDA Medical Device Recalls (openFDA)
J T Posey Company: Posey Connecting Strap/Belt, Polypropylene, 36" (235036). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others.
- Recall number
- Z-2262-2009
- Recalling firm
- J T Posey Company
- Product
- Posey Connecting Strap/Belt, Polypropylene, 36" (235036). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others.
- Status
- Terminated
- Initiated
- 2009-04-20
- Posted
- 2009-09-22
- Terminated
- 2012-04-11
- Reason
- Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others.
- Root cause
- Employee error
- Action
- JT Posey Company issued an "Urgent Medical Device Recall (Removal)" letter dated May 14, 2009 informing customers of the affected products. Any used and/or existing inventory subject to this recall is requested to be returned to Posey including the Recall Reply Fax-Back Form. For further questions, contact your local sales representative or JT Posey Company at 1-800-447-6739 extension 111.
- Quantity
- 131
- Distribution
- Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands.
- Lot, serial or model codes
- All Product with Catalog Number 235036 manufactured between Ferbruary 2009 and April 2009.
- 510(k) numbers
- ["K963436"]
- PMA numbers
- not on file
- Product code
- FMQ
- Firm FEI
- 3016004577
- Firm city
- Arcadia
- Firm state
- CA
- 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