Recall archive
36 recalls · page 2 of 2
Reported Mar 16, 2016
Stryker Position Pro Mattress. Mattress, Air Flotation, Alternating Pressure. PositionPRO is a powered pressure relief…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — Potential for power cord to melt; hazards include electric shock and fire.
FDA (openFDA device enforcement)
Reported Dec 9, 2015
Two-stage and three-stage I.V. poles are shipped as an optional accessory to a bed or stretcher. The I.V. poles are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product details — It was identified by a customer complaint that some I.V. poles were retracting/lowering from an extended position to the low height unexpectedly. An…
FDA (openFDA device enforcement)
Reported Aug 6, 2014
InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details · Reason for recall — Stryker has received complaints from the field alleging instances where the In Touch beds are hoisted or lifted from the floor and the casters have…
FDA (openFDA device enforcement)
Reported Feb 12, 2014
The Gaymar Medi-Therm device provides a means of regulating patient temperature by supplying temperature-controlled…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Reason for recall — Stryker Medical has identified that on some units of the MTA7900, there is a lack of a water temperature display while the unit is in Auto mode.…
FDA (openFDA device enforcement)
Reported Jan 8, 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.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · 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.…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 27, 2013
Model FL14E Rose BedsThe Rose Bed is an AC-powered adjustable long-term care bed intended for medical purposes that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — It was reported that the siderail may appear latched when it is not, due to lack of proper preventive maintenance. This might result in bruises…
FDA (openFDA device enforcement)
Reported Oct 2, 2013
The FL23SE Bed is an AC-powered adjustable hospital bed with four built-in electric DC motors and remote controls that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product details — The nurse call cable (Part Number: QDF23-0571) on the FL23SE Bed is located right under the opening of the bed head box. If an accessory (i.e. IV…
FDA (openFDA device enforcement)
Reported Aug 21, 2013
IsoGel AIR 84, Support Surface. Intended to assist in improving human patient outcomes.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Complaints were received from the field indicating that some Air Pumps were flashing and alarming when connected to the IsoGel AIR" surface upon…
FDA (openFDA device enforcement)
Reported Jan 9, 2013
Medical Surgical Bed, Model 3002SEX Medical Surgical Bed The S3" MedSurg Bed, is intended to support and transport…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details · Reason for recall — Stryker Medical Model 3002S3EX and Model 3005S3EX beds built between March 15, 2012 and May 23, 2012. The affected beds may have been built with…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 26, 2012
The Stryker Model 6390, Power-LOAD, is a power-loading cot fastener system designed to lift, lower, or steer ambulance…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — Model 6390 Power-LOAD systems built between September 12, 2012 and September 27, 2012 may have been built with a load switch slide that does not meet…
FDA (openFDA device enforcement)
Reported Aug 29, 2012
Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair models EMS, EMS24, HHC, and INO Powered MOV…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Reason for recall — Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and distributor of patient transport devices, merged with an affiliate of…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 4, 2012
GoBed+ . Model FL20E Beds are intended for medical purposes in both general patient care as well as critical care…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — An adverse trend of scale and bed exit service reports/complaints were detected for the GoBed+, GoBed II, Rose, and MA204 model beds. Investigation…
4 more products in this recall
FDA (openFDA device enforcement)
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