International Medical Devices Database

Manufacturer Address
J T Posey Company, 5635 Peck Rd, Arcadia CA 91006-5851
Source
USFDA
1 Event
- Recall of Wrist restraint, wrist cuff

One device in the database

Wrist restraint, wrist cuff

Model / Serial
The model/catalog number for the device is 2900. All lots are being recalled.
Product Classification
General Hospital and Personal Use Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide Distribution
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.

One manufacturer with a similar name

Learn more about the data here

J T Posey Company

Manufacturer Address
J T Posey Company, 5635 Peck Rd, Arcadia CA 91006
Manufacturer Parent Company (2017)
Tidi Products Llc
Source
USFDA

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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