FDA Enforcement Class II Terminated

NIO-A / NIO-P is an instant IO access device comprises housing with spring load mechanism that injects a trocar needle into the bone marrow of a patient and allows connection of syringe or IV administration set. The NIO-A is intended for adults above 12 years old and the NIO-P is intended for pediatric patients 3 - 12 years of age.

Recall: Z-2680-2016 · Reported September 7, 2016

Enforcement

Recall Number
Z-2680-2016
Event ID
75008
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Waismed Ltd
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
September 7, 2016
Initiation Date
August 18, 2016
Classification Date
August 27, 2016
Termination Date
December 5, 2016
Address
10, Amal St, N/A, Rosh Haayin, N/A, N/A, Israel

Description

NIO-A / NIO-P is an instant IO access device comprises housing with spring load mechanism that injects a trocar needle into the bone marrow of a patient and allows connection of syringe or IV administration set. The NIO-A is intended for adults above 12 years old and the NIO-P is intended for pediatric patients 3 - 12 years of age.

Reason

WaisMed received a report in which during the operation of the NIO-A, the needle was not released from the device as expected. The device was placed on the floor and after several minutes the needle was released spontaneously. NIO-A and the NIO-P models have the same activation mechanism. However, none of the affected lots of the NIO-A are distributed in the US, and thus the company is only recalling a single lot of NIO-P in the US.

Code Info

1620005

Distribution

WI, TX, CA, LA and the following countries: UK, Spain, Poland, Israel, Czech Republic, France, Belgium, Denmark, Italy, Cyprus, Austria, Greece, Slovenia, Australia, Germany, Estonia, New Zealand, Switzerland, Costa Rica, Guatemala, Canada, Malaysia, Poland, Singapore, Lithuania, Romania

Quantity

50