FDA Recall Terminated

Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.

Recall: Z-0928-2017 · Initiated November 23, 2016

Recall

Recall Number
Z-0928-2017
Event Number
75824
Firm
Allen Medical Systems, Inc. One Post Office Square
FEI Number
1221538
Product Code
HST
Status
Terminated
Root Cause
Under Investigation by firm
Initiated
November 23, 2016
Terminated
August 20, 2019
Address
Acton, MA, 01720

Description

Arthex S3 Arm Sleeve Connector; Catalog Number AR-1650-02; manufactured and distributed between March and November 2016.

Reason

During use, the unit could separate un-expectantly. This failure would allow the patient's arm to fall out of suspension during a procedure, possibly causing moderate injury to the patient. This potential defect is not apparent to the user.

Action

The firm's customer was notified of the recall via letter on November 23, 2016. They were asked to take the following actions: 1. Immediately remove from service your Arthrex S3 Arm Sleeve Connector (AR-1650-02). All serial numbers are impacted. 2. Please follow the included instructions for the return of all S3 Arm Sleeve Connectors (AR-1650-02). Allen Medical will inspect, repair or replace all units as necessary at no cost to you. Please take steps to retrieve the units from your customers and return them to Allen Medical via the standard Return Material Authorization (RMA) process. In order to minimize this inconvenience, we will repair the Arthrex S3 Arm Sleeve Connector and return the device to you as soon as possible. For further questions, please call (978) 266-4280.

Distribution

US Distribution to the state of : FL

Quantity

420 devices