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1,032 catalysts · 1,000 device adverse event · 21 approval · 6 device 510k · 3 device pma · 2 grant

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2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 0 catalysts2026-08-27: 0 catalysts2026-08-28: 30 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 1 catalyst2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts2026-11-09: 1 catalyst2026-11-10: 0 catalysts2026-11-11: 0 catalysts2026-11-12: 0 catalysts2026-11-13: 0 catalysts2026-11-14: 0 catalysts2026-11-15: 0 catalysts2026-11-16: 0 catalysts2026-11-17: 0 catalysts2026-11-18: 0 catalysts2026-11-19: 0 catalysts2026-11-20: 0 catalysts2026-11-21: 0 catalysts2026-11-22: 0 catalysts
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  • device adverse event1,000
  • approval21
  • device 510k6
  • device pma3
  • grant2
therapy area

no tagged catalysts yet

Week of Mar 30, 2026

50
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUICK SET — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoCONTACT DETACH — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoINSET GUARD — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Battery Problem; Power Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMENTOR SMOOTH ROUND HIGH PROFILE — Injury event

Material Rupture

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Wireless Communication Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem; Appropriate Term/Code Not Available

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoULTIPACE¿ LEAD, 65CM MRI — Injury event

Device Dislodged or Dislocated

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoESSURE — Injury eventBayer AG

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK SPHERE TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoM.U.S.T. RODS — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoSHOULDER SYSTEM — Injury event

Device Dislodged or Dislocated

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK PRIMARY TOTAL KNEE SYSTEM — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoAMISTEM H FEMORAL STEMS — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK PRIMARY TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK PRIMARY TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoSMS STEM — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK SPHERE TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK TOTAL KNEE SYSTEM — Injury event

Loosening of Implant Not Related to Bone-Ingrowth

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK SPHERE TOTAL KNEE SYSTEM — Injury event

Device Appears to Trigger Rejection

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoAMISTEM H FEMORAL STEMS — Injury event

Implant subsidence

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoSHOULDER SYSTEM — Injury event

Osseointegration Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoDM CONVERTER ¿ TIN COATED — Injury event

Device Dislodged or Dislocated

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoSHOULDER SYSTEM — Injury event

Device Dislodged or Dislocated

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoGMK REVISION TOTAL KNEE SYSTEM — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoRESERVOIR 3ML MMT-332A — Injury event

Improper Flow or Infusion

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoUNKNOWN GEL IMPLANTS — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoTITANIUM PORT — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoIMPLANTED PORT — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoPOWERPORT SLIM IMPLANTABLE PORT, CHRONOFLEX SINGLE-LUMEN, KIT, 6F — Injury event

Obstruction of Flow

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoPOWERPORT SLIM IMPLANTABLE PORT — Injury event

Fracture; Migration

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoQUARTET — Injury event

Failure to Capture; Device Dislodged or Dislocated

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
›Mar 31, 2026device adverse event151d agoMINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL — Injury event

Adverse Event Without Identified Device or Use Problem

full page →fda device maude ↗
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