Recall archive
36 recalls · page 1 of 2
Reported Mar 25, 2026
Cub Pediatric Crib, Model FL19H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Cribs sold in the USA are missing two access door warning labels.
FDA (openFDA device enforcement)
Reported Dec 17, 2025
Stryker MV3 bariatric bed, Part Number 5900000001
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 issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
ProCuity bed series, model number 3009, item number: 300900000000,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Patient beds are missing test values for electrical safety tests presenting risk of tissue burn or electrical shock.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 19, 2023
Power-PRO 2- A powered ambulance cot that consists of a platform, including a mattress, mounted on a wheeled,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Base leg assembly may bend and result in difficulty engaging/disengaging from fastener, difficulty loading/unloading from ambulance, difficulty…
FDA (openFDA device enforcement)
Reported Mar 22, 2023
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of…
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting…
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Transport Stretcher 747 - a non-powered, wheeled device designed to support patients in a horizontal position, Part…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Reason for recall — Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The…
18 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2020
Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — Connector between support surface and pump may be out of tolerance resulting in difficulty in removing the CPR connector causing a delay in…
FDA (openFDA device enforcement)
Reported May 20, 2020
Stryker Power-PRO TL cot-powered ambulance cot Model Number 6550 - Product Usage: is a powered wheeled stretcher that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — Ambulance Cots may not meet crash test standard BS EN 1789
FDA (openFDA device enforcement)
Reported May 22, 2019
Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Naera Hospital Bassinet, Model No. 4402
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Reason for recall — It was identified that the volume of air inside the mattress may expand in regions of high altitude which may result in an unintended gap between the…
FDA (openFDA device enforcement)
Reported Nov 21, 2018
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — The beds with the high rail side rail option may not be complaint with IEC 60601-2-52/C1:2010. There is a potential risk of entrapment.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2018
Altrix¿ Precision Temperature Management System Model: 8001Product Usage: The Altrix system is intended for circulating…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Users may experience alarm fatigue due to frequent alarming relating to patient temperature deviation beyond 0.5¿C while in Automatic mode. 2. Users…
FDA (openFDA device enforcement)
Reported Sep 26, 2018
IsoFlex LAL Support Surface, Model Number 2860 Product Usage: : The IsoFlex LAL support surface assists in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product details — Certain 2860 IsoFlex LAL support surfaces were assembled with a non-conforming fire barrier.
FDA (openFDA device enforcement)
Reported May 9, 2018
6376 M-1 Cot Fastener, catalog no. 6376000000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — The Operations Manual and Maintenance Manual are missing various warnings and contain incorrect information.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 25, 2018
Power-LOAD Cot Fastening System, Model #6390, Catalog #6390-000-000, UDI: 07613327261523 Power-LOAD is intended to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product details — The power load floor plates which hold the ambulance cot anchors in place during patient transport, may be broken.
FDA (openFDA device enforcement)
Reported Mar 21, 2018
T/Pump temperature therapy pump, Models TP700 and TP700C
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Stryker Medical Division
Matched: Brand — The T/Pump Operations Manual and Maintenance Manual were incorrectly revised to add the sentence, Temperature therapy can also be for heat…
FDA (openFDA device enforcement)
Reported Feb 7, 2018
MA3320-PM Premium Adult - SYK Mistral-Air Premium Blankets. MODEL #: MA3302-PM. CATALOG #(s): MA3302-PM
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — It was identified that the Mistral-Air Premium blankets may be capable of conducting electricity during a defibrillation or cardioversion therapy at…
FDA (openFDA device enforcement)
Reported May 17, 2017
Medi-Therm Hyper/Hypothermia System, MTA7900
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — The water may reheat too quickly if the unit is in "Automatic" mode, switched to "Manual" mode to view water temperature, and then switched back to…
FDA (openFDA device enforcement)
Reported Dec 21, 2016
Performance-LOAD Ambulance Cot Fastener Stretcher, Wheeled
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Reason for recall — Stryker Medical initiated a voluntary recall of Stryker Performance-LOAD Cot Fasteners due to complaints that fastening system may not have been…
FDA (openFDA device enforcement)
Reported Aug 17, 2016
S3 MedSurg Bed, Model 3005. Stryker Medical
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — CPU board failures cause fowler (backrest) electronic controls to stop working.
FDA (openFDA device enforcement)
Reported Jun 22, 2016
Stryker PowerPRO (XT, IT, or TL) Cots Stretcher, Wheeled The Stryker Power-PRO" are powered ambulance cots are designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand · Product · Product details — Complaints of smoke coming from the foot end of the cot. This reportedly occurred when either the battery was placed into the cot or shortly after…
FDA (openFDA device enforcement)
Reported May 4, 2016
Spirit One A-C Powered Hospital Bed
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — Customer complaints associated with faulty brake system
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
Matched: Brand — The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001, and 0753-002-001) were manufactured using the incorrect oil. The oil…
1 more product in this recall
FDA (openFDA device enforcement)
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