FDA Device Intelligence
HomeST. JUDE MEDICAL, INC. › TactiSys™ Quartz Equipment

TactiSys™ Quartz Equipment

ST. JUDE MEDICAL, INC. · Model TSM-BSD-GBL · UDI-DI 05415067029348

OAE Prescription
0
510(k) clearances
11,466
Adverse events (349 deaths)
34
Recalls
64
Facilities

Description

Tactisys to Precision Beside Mounting Bracket

Recalls

DateFirmReason
2025-09-10AbbottAbbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
2025-09-10AbbottAbbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
2025-09-10AbbottAbbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
2025-09-10AbbottAbbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
2025-09-10AbbottAbbott has become aware of a limited number of tip detachment events during catheter removal from the packaging.
2025-02-07CardioFocus, Inc.Damage to the sterile barrier pouch of catheter, which could potentially compromise its sterility.
2024-10-10Boston Scientific CorporationBoston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
2024-10-10Boston Scientific CorporationBoston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
2024-10-10Boston Scientific CorporationBoston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
2024-10-10Boston Scientific CorporationBoston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.