Z-1542-2014 Class II Terminated
FDA device recall Z-1542-2014 was initiated by Med-Mizer, Inc. on April 18, 2014 and is designated Class II. Reason for recall: All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support … The recall status is terminated (terminated May 23, 2016). Affected quantity: 1.
Recall Details
- Product Type
- Devices
- Report Date
- May 14, 2014
- Initiation Date
- April 18, 2014
- Termination Date
- May 23, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1
Product Description
RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 799, 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
Reason for Recall
All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating from the frame. If the weld on the tube breaks, it can lead to bed collapse or the rollers coming out of the channel on th
Distribution Pattern
USA (nationwide)
Code Information
Serial Number 2000