Z-2264-2009

Posey Connecting Strap/Belt, Polypropylene, 60" (235060). Intended for medical purposes to limit a patient's...

Name: Z-2264-2009 Posey Connecting Strap/Belt, Polypropylene, 60" (235060). Intended for medical purposes to limit a patient's...
Creator: J T Posey Company
Published: 2009-04-20
License: https://open.fda.gov/license/

J. T. Posey Co. / initiated 2009-04-20 / Terminated / root cause: manufacturing process

FDA source

J T Posey Company began a recall of Posey Connecting Strap/Belt, Polypropylene, 60" (235060). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment... on 2009-04-20. The reason FDA records is "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...". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-2264-2009
Status: Terminated
Initiated: 2009-04-20
Posted: 2009-09-22
Terminated: 2012-04-11
Recalling firm: J. T. Posey Co.
Product: Posey Connecting Strap/Belt, Polypropylene, 60" (235060). Intended for medical purposes to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others.
Product code: FMQ Restraint, Protective
Reason for recall: 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 tag: manufacturing process
FDA 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 in commerce: 45
Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands.
Product codes and lots: All Product with Catalog Number 235060 manufactured between Ferbruary 2009 and April 2009.

Product code FMQ

K963436Class IRestraint AccessoriesJ. T. Posey Co. / cleared 1996-11-22

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)