FDA Device recall Z-1071-2013
Posey Biothane Restraint Cuffs, Catalog Number 2900
- FDA Device
- Class II
- terminated
- Published 2013-04-17
On 2013-04-17 the FDA classified a Class II recall of Posey Biothane Restraint Cuffs, Catalog Number 2900 by J T Posey, citing 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 t….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1071-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-31 |
| Published | 2013-04-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | J T Posey |
| Distribution | US |
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.
Reason
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.
Identifiers
| code_info | The model/catalog number for the device is 2900. All lots are being recalled. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1071-2013%22
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