FDA Device Intelligence
HomeCoopersurgical, Inc. › Koh Cup

Koh Cup

Coopersurgical, Inc. · Model KCS-40 · UDI-DI 00888937015751

HEW Prescription
10
510(k) clearances
251
Adverse events
4
Recalls
22
Facilities

Description

Koh Cup 4.0 cm Stainless Steel Vaginal Fornices Delineator

Recalls

DateFirmReason
2021-04-23CooperSurgical, Inc.The affected Koh Cup were incorrectly packaged with a 3.5cm Ultem Koh cup, P/N 34131-04, instead of a 3.0cm Ultem Koh cup, P/N 34131-03 as required.
2019-06-14CooperSurgical, Inc.The soft, flexible cup of the Advincula Delineator may be unvalidated and could potentiall crack when subjected to excessive compressions during use, leading to serious health cons
2019-06-14CooperSurgical, Inc.The soft, flexible cup of the Advincula Delineator may be unvalidated and could potentiall crack when subjected to excessive compressions during use, leading to serious health cons
2018-09-04CooperSurgical, Inc.The seal of the sterile pouch may be compromised, thereby increasing the risk of infection.

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.