FDA-Device2013-04-17Class II
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.
J T Posey Company
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.
Sold states
Nationwide Distribution
Affected count
1673 units
Manufactured in
5635 Peck Rd, Arcadia, CA, United States
Products
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.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1071-2013Don't want to check this manually?
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