FDA Device recall Z-0617-2014
Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals
- FDA Device
- Class II
- terminated
- Published 2014-01-08
On 2014-01-08 the FDA classified a Class II recall of Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals by Stryker Medical Division, citing stryker Medical has identified a potential issue associated with Secure II and S3 Med/Surg beds built between April 2nd, 2005 and July 26th, 2011. The affected beds have the poten….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0617-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-26 |
| Published | 2014-01-08 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Medical Division |
| Distribution | US |
Product
Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals. The bed is designed for a 15 year expected service life under normal use conditions, and with appropriate periodic maintenance as described in the maintenance manual for each device. There are minimal differences between the functionality of the two models, each of which function as a highly complex system of a large number of individual components.
Reason
Stryker Medical has identified a potential issue associated with Secure II and S3 Med/Surg beds built between April 2nd, 2005 and July 26th, 2011. The affected beds have the potential to experience damage to the Foot End Cover and/or Power Coil Cable due to reduced clearance between the Foot End Cover and Foot End Lift Header.
Identifiers
| code_info | Models: 3002 EX, 3002 KCI, 3002 CUSTOM, 3002 ZOOM, 3002000000, and 3002 ZX-SB. And Serial Numbers: 060215711 , 06021…Models: 3002 EX, 3002 KCI, 3002 CUSTOM, 3002 ZOOM, 3002000000, and 3002 ZX-SB. And Serial Numbers: 060215711 , 060215712 , 060215713 , 060215714 , 060215715 , 060215716 , 060215717 , 060215718 , 060215719 , 060215720 , 060215721 , 060215722 , 060215723 , 060215724 , 060215725 , 060215726 , 060215727 , 060215728 , 060215729 , 060215730 , 060215731 , 060215732 , 060215733 , 060215734 , 060215735 , 060215736 , 060215737 , 060215738 , 060215739 , 060215740 , 060215741 , 060215742 , 060215743 , 060215744 , 060215761 , 060215762 , 060215763 , 060215764 , 060215765 , 060215766 , 060215767 , 060215768 , 060215769 , 060215770 , 060215771 , 060215772 , 060215773 , 060215774 , 060215775 , 060215776 , 060215777 , 060215778 , 060215779 , 060215780 , 060215781 , 060215782 , 060215783 , 060215784 , 060215785 , 060215786 , 050916199 , 060515187 , 080615291 , 080615292 , 0806 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0617-2014%22
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