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21 thg 9, 2026•1 phút đọc
MFDS recalls 4 hand sanitizers after content non‑compliance in nationwide test
The Korean Food & Drug Administration tested 100 top‑selling hand sanitizers and found four failing the ingredient‑content standards, prompting sales suspension, recall and disposal.
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16 thg 9, 2026•1 phút đọc
Medtronic Identifies Reflective Material Variation in Sterile Passive Spheres
Health Canada reports a limited number of Medtronic sterile passive spheres have variable reflective coating that could affect navigation system tracking.
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16 thg 9, 2026•1 phút đọc
Medtronic Alerts Variation in Reflective Material on Passive Spheres May Impact Navigation Tracking
Medtronic reports a variation in the reflective coating of certain sterile passive spheres, which could affect instrument detection and tracking during navigation procedures.
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7 thg 9, 2026•1 phút đọc
AlpBio Executive Receives MFDS Director Award for Functional Food Contributions
AlpBio’s marketing executive Nomi Seon was honored with the MFDS Director’s Award for his 25‑year contributions to the health functional food industry.
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5 thg 9, 2026•1 phút đọc
Korean pharma firms recall batches of diabetes drugs and antiemetics over quality issues
Domestic manufacturers have issued voluntary recalls for certain batches of diabetes treatments and anti‑emetic tablets after detecting contamination, potency failures and impurity exceedances.
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4 thg 9, 2026•1 phút đọc
Stryker LifePak R-35 Monitor-Defibrillator May Have Improperly Seated Connectors
Stryker discovered that some LifePak R-35 units may have printer and modem access port connectors not fully seated, potentially appearing flush or recessed.
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4 thg 9, 2026•1 phút đọc
Gore Reports Quality Issue with VIABAHN® Devices Potentially Affecting Tip Bonding
Gore discovered some VIABAHN® devices were processed on equipment outside the validated range, potentially causing incorrect distal tip bonding.
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4 thg 9, 2026•1 phút đọc
Gore VIABAHN® Device Quality Issue Identified
Gore discovered some VIABAHN® devices were processed on equipment outside validated range, risking incorrect distal tip bonding.
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3 thg 9, 2026•1 phút đọc
Balt Extrusion Recalls ANRYV Connectors Over Endotoxin Test Issue
Balt Extrusion is voluntarily recalling certain ANRYV connector lots after bacterial endotoxin test failures; no patient harm reported.
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3 thg 9, 2026•1 phút đọc
Balt Extrusion Voluntarily Recalls ANRYV Connectors Over Bacterial Endotoxin Test Failure
Balt Extrusion is voluntarily recalling specific ANRYV connector lots after non‑conforming bacterial endotoxin test results, affecting standalone connectors and those in selected kits; no patient harm reported.
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31 thg 8, 2026•1 phút đọc
Korean Medicine Committee Urges International Decoction Oversight
The Korean Medical Association’s Korean Medicine Countermeasure Special Committee demands international‑standard oversight of external decoction rooms after a police‑investigated insurance fraud involving pre‑manufactured herbal prescriptions.