J T Posey Company: Medical Device Recall in 2013 - (Recall #: Z-1071-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit a patient's movement to the extent necessary for treatment or protection of the patient or others.

Product Classification:

Class II

Date Initiated: October 31, 2012

Date Posted: April 17, 2013

Recall Number: Z-1071-2013

Event ID: 63622

Reason for Recall:

The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900, that did not meet the required specifications for tensile strength. Failure of these rivets could allow the cuff to become disconnected from the connecting strap and allow patients to regain free use of the limb.

Status: Terminated

Product Quantity: 1673 units

Code Information:

The model/catalog number for the device is 2900. All lots are being recalled.

Distribution Pattern:

Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated