Oculus Myopia Master , Ref 68100, CE 0123
Oculus Optikgeraete GMBH
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
🏥 Medical Devices • 15,809 recalls
Oculus Optikgeraete GMBH
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Loss of availability of the wireless foot switch during procedures.
Oculus Optikgeraete GMBH
Their is a potential that optical devices with insufficient anti-reflective coating may lead to incorrect axial length measurements.
Olympus Corporation of the Americas
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Olympus Corporation of the Americas
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Olympus Corporation of the Americas
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
An issue was found in Software RayCare 5A, 5B, 6A, including service packs, where an allergy warning against medication substance (drug ingredient) will not be displayed as expected under certain circumstances
Olympus Corporation of the Americas
Complaint of endoscope model becoming lodged in the endotracheal tube connector due to diameter being too large.
Smiths Medical ASD
Smiths Medical identified a labeling error in which the barcode (UDI) was not correctly reflecting the expiration date of the product
Olympus Corporation of the Americas
The air/water valve MAJ-1444 used with OER-Pro and OER-Elite may become damaged and result in loss of the one-way valve functionality by repeated automated endoscope reprocessing in Olympus OER machines, causing body fluid could backflow into the air/water channel of the ultrasonic endoscopes during the procedure.
Medicrea International
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Medicrea International
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Medicrea International
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Smith & Nephew
A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on the product label.
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.
Smith & Nephew
A complaint was received indicating that a package contained a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 40CM 130 DEGREE LEFT implant instead of a TRIGEN TROCHANTERIC ANTEGRADE NAIL LIME 11.5MM X 36CM 130 DEGREE LEFT as described on the product label.