device recall
saveGE Healthcare device recall (Cls II)
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GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological — Reason: Under certain workflows, patient information shown in the viewer may not match the images displayed on Centricity Universal Viewer Zero Footprint Client (ZFP) with versions ZFP v6.0: SP11.6, SP11.6.0.1 and SP11.6.1 on systems with Patient Timeline installed, — Status: Ongoing
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same company · ±60 days · 6
- device 510kGE Healthcare — View (510k cleared)Jan 8, 2026
- device 510kHR Healthcare — EZ-Protect Hydrophilic Closed System Intermittent Catheter; EZ-Protect Hydrophilic Closed System Intermittent Catheter Kits (510k cleared)Jan 29, 2026
- device recallLSL Healthcare Inc. device recall (Cls II)Dec 22, 2025
- approvalCLARISCAN: CLARISCAN (GADOTERATE MEGLUMINE) — FDA approvalDec 15, 2025
- approvalCLARISCAN: CLARISCAN (GADOTERATE MEGLUMINE) — FDA approvalDec 15, 2025
- approvalCLARISCAN: CLARISCAN (GADOTERATE MEGLUMINE) — FDA approvalDec 15, 2025
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