S3 Med/Surg Bed Secure II and the 3002 S3 are the beds typically… — Class II medical device recall Z-0618-2014
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2014-01-08, distributed nationwide. Stryker Medical has identified a potential issue associated with Secure II and S3 Med/Surg beds built between
| Recall number | Z-0618-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2013-11-26 |
| Classified | 2013-12-31 |
| Reported by FDA | 2014-01-08 |
| Terminated | 2015-05-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AR, BR, CA, CL, CN, DE, GB, KR, MX, SG |
| Quantity | 108,769 total |
| Serial numbers | 080615928, 080615942, 080615956, 080616016, 080616524, 080616525, 080715001, 080715002, 080715003, 080715004, 080715005, 080715006, 080715007, 080715008, 080715009, 080715010, 080715011, 080715012, 080715013, 080715014, 080715015, 080715016, 080715017, 080715018, 080715019 and 475 more |
| Model numbers | 3002 |
Product
S3 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 for recall
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.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.