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J T Posey Company recalls Posey Biothane Restraint Cuffs, Catalog Number 2900. The device is intended to limit a patient's movement to the exte
Recalled April 17, 2013 · FDA recall Z-1071-2013 · J T Posey
Hazard
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. · FDA Class II
Units
1673 units
Sold at
Nationwide Distribution
Description
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.
Product
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.
Manufacturer(s)
J T Posey Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →