U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
The Parent Company was added by ICIJ.
The parent company information is based on 2017 public records.
데이터 추가 비고
Lift, Patient, Non-Ac-Powered - Product Code FSA
원인
The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. this could cause an unsafe transfer. patient may fall.
조치
Liko notified Distributors of the recall by letter on 1/9/06 via UPS and provided replacement Slingbars Version 2.
Expanded Recall:
On 6/20/06, Liko sent a 2nd recall letter expanding the recall to additonal serial numbers via Certified Mail.