Reported Jan 8, 2014 · Terminated
Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals.…
Stryker Medical Division of Stryker Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Medical Division of Stryker Corporation · 3800 E Centre Ave · Portage, MI · 49002-5826
Is this the product you have?
- 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.
- Lot codes and dates
- Models
3002 EX3002 KCI3002 CUSTOM3002 ZOOM3002000000and 3002 ZX-SB
- And Serial Numbers
2,322 of 2,322 codes
060215711060215712060215713060215714060215715060215716060215717060215718060215719060215720060215721060215722060215723060215724060215725060215726060215727060215728060215729060215730060215731060215732060215733060215734060215735060215736060215737060215738060215739060215740060215741060215742060215743060215744060215761060215762060215763060215764060215765060215766060215767060215768060215769060215770060215771060215772060215773060215774060215775060215776060215777060215778060215779060215780060215781060215782060215783060215784060215785060215786
- Models
- Amount recalled
- 108,769 Total
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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