Search U.S. Product Recalls Database

Showing 5361–5380 of 8393 results

Sort:

Steris Light Handle Cover (Steris) – detachment risk (2023)

Light handle covers may separate from the light handle (detach and fall off) during use, this could result in a procedure delay and/or impact the sterile field which could result in an injury to the patient

Moderate

FDAMar 17, 2023Nationwide• Steris Corporation

Spectral CT 7500 System (Philips) – foot switch entrapment (2023)

Laceration Risk

Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operators foot. If foot or leg entrapment occurs while pressing Unload Pedal, the risk to operators may include: pain, muscle or ligament sprain, abrasion, laceration, contusion, fracture, loss of function, and joint dislocation.

High

FDAMar 17, 2023Nationwide

Stay Informed

Search Product Recalls

Steris Light Handle Cover (Steris) – detachment risk (2023)

Spectral CT 7500 System (Philips) – foot switch entrapment (2023)

Medtronic SenSight Tunneler Kit (Medtronic) – carrier machining issue (2023)

CryoTreQ Surgical Device (Beaver Visitec) – disassembly risk (2023)

V. Mueller Graves Speculum (Carefusion) – product mismatch (2023)

ADVIA Centaur Cortisol Test (Siemens) – urine sample bias (2023)

JULIET Lumbar Plate (SpineArt) – potential disassembly (2023)

Integre Pro Laser Device (Ellex) – beam scattering risk (2023)

Atellica IM Cortisol Test (Siemens) – urine sample bias (2023)

Beckman Coulter Access Free T3 (Beckman Coulter) – test result issue (2023)

Hamilton-C6 Ventilator (Hamilton Medical) – safety ventilation error (2023)

VITROS 5600 Integrated System (Ortho-Clinical Diagnostics) – MicroTip Pack Issue (2023)

Alinity h Interface Module (Inpeco) – sample ID mis-association (2023)

Vesmatic Cube 80 Interface Module (Inpeco) – Sample ID Mismatch (2023)

VITROS XT 7600 Integrated System (Ortho-Clinical Diagnostics) – MicroTip Pack Issue (2023)

Alcon Custom Pak Surgical Pack (Alcon) – Incomplete Seals (2023)

Stryker MAKO Baseplate Trial (Howmedica) – incorrect size marking (2023)

Input Output Module (Inpeco) – sample ID mis-association (2023)

MAKO RESTORIS MCK Baseplate Trial (Stryker) – Incorrect Size Marking (2023)

PVT Interface Module (Inpeco) – sample ID mis-association (2023)