FDA Device Intelligence
HomeCOOK INCORPORATED › Malecot

Malecot

COOK INCORPORATED · Model G14526 · UDI-DI 00827002145269

KOB Prescription
10
510(k) clearances
205
Adverse events (1 deaths)
66
Recalls
23
Facilities

Description

Malecot Nephrostomy Catheter/Stent Set

Recalls

DateFirmReason
2019-04-22Cook Inc.Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting.
2019-04-22Cook Inc.Kwart RetroInject Stent Set (Multi-Length) and Salle Intraoperative Pyeloplasty Stent Set Instructions for Use (IFU) did not include a warning for stent knotting.
2019-01-04Cook Inc.The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
2019-01-04Cook Inc.The wire guide may be incorrectly loaded into the wire guide holder, leading to the stiff tip of the wire guide being introduced into the patient instead of the flexible tip.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.
2005-07-22Boston Scientific CorporationThe Tearaway Introducer Sheath may have cracked hubs/handles and/or improper peeling during use.

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.