Recall of batch 272955 of the IVD General Medical Device, Kits STACK Prest. 20 July 2026 Medical technologyMedical device recallsHealth professionals 20 Jul 2026
Decision prohibiting the movement and disposal – 92890 Cotton absorbent gauze (REF: 6-1003Ν2 & REF: 6-1006Ν2) 20 July 2026 Medical technologyMedical device recalls 20 Jul 2026
Recall of batches of the medical device reagent 'CHORUS Ttg-G' 10 July 2026 Medical technologyMedical device recallsHealth professionals 10 Jul 2026
Recall of batches of MDD Class III medical devices, Surgipro, Surgipro II, Dermalon, V-Loc 90 and V-Loc 180 sutures 10 July 2026 Health professionalsMedical technologyMedical device recalls 10 Jul 2026
Recall of batches of the MDD Class IIa Medical Device, THERAKOS CELLEX Photopheresis Procedural Kit 8 July 2026 Medical technologyMedical device recallsHealth professionals 08 Jul 2026
Recall of batches of the Rapid Refill Continuous Injection System Medical Device 8 July 2026 Medical technologyMedical device recallsHealth professionals 08 Jul 2026
Recall of the batches in the table below, of the MDD Class IIa Medical Device, EORA Arterial Cannulas 3 July 2026 Medical technologyMedical device recallsHealth professionals 03 Jul 2026
Recall of serial numbers 109980699 and 110143347 of code 1739994, of the MDD Class I Medical Device, Adapter for Head positioning. 3 July 2026 Medical technologyMedical device recallsHealth professionals 03 Jul 2026
Recall from the market of products with Device name: "Non-sterile folded gauze", manufactured by YANCHENG ZAICHUANG MEDICAL SUPPLIES CO LTD (China) (Authorized Representative for the EU MedPath GmbH (Germany)), which are accompanied by a falsified declaration of conformity from the manufacturer. 2 July 2026 Medical technologyMedical device recalls 02 Jul 2026
Recall of the batches of the MDD Class III Medical Device, HYBRID Guidewire, listed in the table below June 29 2026 Medical technologyMedical device recallsHealth professionals June 29, 2026