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Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation Recalls

All product recalls associated with Stryker Medical Div. of Stryker Corporation.

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Recall Summary

Total Recalls

1000

Past Year

730

Class I (Serious)

175

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 9641–9660 of 11124 recalls

Stryker Medical Div. of Stryker Corporation: Stryker Medical transport stretcher, Stryker Medical, Por...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Zoom critical care bed, 115v, Stryker Medical, Po...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Epic II critical care bed, 115v, Stryker Medical,...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDA

1...481 482483484 485...557

Page 483 of 557Next

Aug 10, 2009

Nationwide

• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical cam bearing service parts, Stryker Medica...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Ossur H F Grjothals 5 Reykjavik Iceland: Total Knee Junior Model Number 1100 Product Usage: The T...

Some units of the Total Knee Junior produced between November 25th, 2008 and through April, 2009 contain balancing units that may fail under extreme use over a long period. The fault is noncritical and no incidents or injuries resulting from this situation have been reported to Ossur at this stage. Over long term use (estimated to be in the four to six year range) the prosthetic device may fail a

FDAAug 10, 2009Nationwide• Ossur H F Grjothals 5 Reykjavik Iceland

Stryker Medical Div. of Stryker Corporation: Stryker Secure II MedSurg bed, 115 v, Stryker Medical, Po...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker MedSurg bed, 115v, Stryker Medical, Portage, MI; ...

The backrest of the bed may not stay in an upright position (may drift down when left raised).

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical M-Series stretcher, Stryker Medical, Port...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical eye surgery stretcher, Stryker Medical, P...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical trauma stretcher, Stryker Medical, Portag...

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Stryker Medical Div. of Stryker Corporation: Stryker Medical , Model 722. Wheeled hospital stretcher.

The brake/steer pedal may seize, resulting in the brakes not working.

FDAAug 10, 2009Nationwide• Stryker Medical Div. of Stryker Corporation

Medtronic Vascular Galway Limited Parkmore Business Park West Galway Ireland: Endeavor Resolute Zotarolimus-Eluting Coronary Stent Syst...

The product was removed from investigational sites due to a packaging issue, in that the device units were packed without the foil pouch, oxygen absorber and Instructions For Use.

FDAAug 6, 2009Nationwide• Medtronic Vascular Galway Limited Parkmore Business Park West Galway Ireland

Black & Decker Grasshog XP String Trimmer/Edgers (Black & Decker) – laceration risk (2009)

Fire/Burn Risk

The Black & Decker GH1000 Grasshog XP String Trimmers/Edgers are electric-powered. Trimmer/edgers with date codes 200546 through 200645 (representing manufacture dates of November 14, 2005 through November 6, 2006) are included in this recall. The date code is located on the underside of the trimmer/edger's handle. Only trimmers with black spool caps are included in the recall. Those with orange spool caps are not included in the recall.

CPSCAug 4, 2009Nationwide• Black & Decker (U.S.) Inc., of Towson, Md.

Stryker Imaging: Guardian Services, Guardian Software, Part Number 0240-00...

Guardian Services data backup does not contain 100% data for all OrthoPad customers on a daily basis.

FDAAug 3, 2009Nationwide• Stryker Imaging

Beckman Coulter Inc.: Active Prolactin ELISA, 96 Wells, DSL-10-4500 The DSL-10...

The recall was initiated because Beckman Coulter has confirmed that the Active Prolactin ElLISA kit, lot number 890291 over estimates the expected dose values for patient serum samples due to a shift in the assigned calibrator values. Beckman Coulter recommends that patient results generated with the affected lot be evaluated in the context of other diagnostic tests and the clinical presentatio

FDAAug 3, 2009Nationwide• Beckman Coulter Inc.

Stryker Imaging: Guardian Services, Part Number 0240-009-430 with Part Num...

Product serving as data backup protection does not contain 100% data backup for all NetPractice customers on a daily basis.

FDAJul 31, 2009Nationwide• Stryker Imaging

Elekta, Inc.: iView GT Electronic Portal Imaging Device, used with radi...

Image problems that have an effect on patient position corrections and on the accuracy of the radiation treatment.

FDAJul 31, 2009Nationwide• Elekta, Inc.

Little Tikes Clubhouse Swing Set (Little Tikes) – fall hazard (2009)

The Little Tikes Clubhouse Swing Set is a plastic molded product that features a climbing wall, rope ladder, slide and two swings with blue and yellow seats. Only the blue seat model is being recalled. The model numbers are 400V and 612398.

CPSCJul 30, 2009Nationwide• Little Tikes, of Hudson, Ohio

Beckman Coulter Inc.: Unicel DxH 800 Coulter Cellular Analysis System, Part num...

The recall was initiated after Beckman Coulter confirmed an issue with the UniCel DxH 800 during in-house testing. It was determined that there is a potential for a false increase in platelet results, due to micro-bubbles. This situation could present a risk of falsely increased platelet results in patient samples as diluent containers are depleted.

FDAJul 28, 2009Nationwide• Beckman Coulter Inc.

Stryker Endoscopy: Stryker Endoscopy PrepStrap Shoulder Sleeve, Model Number...

Undeclared Allergen

Latex-- Certain lots of Product contain undeclared latex.

FDAJul 27, 2009Nationwide• Stryker Endoscopy