Home › Device types › EZQ
Pouch, Colostomy
FDA product code EZQ · Class 1 · Gastroenterology, Urology
141
Registered devices
2,020
Adverse events
5
Recalls
6
510(k) clearances
Devices with this code
ACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTESTEEM+ — CONVATEC, PURCHASING DEPARTMENTFLEXI-SEAL — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTESTEEM SYNERGY — CONVATEC, PURCHASING DEPARTMENTNATURA — CONVATEC, PURCHASING DEPARTMENTESTEEM SYNERGY+ — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTNATURA+ — CONVATEC, PURCHASING DEPARTMENTACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTESTEEM+ — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTNATURA+ — CONVATEC, PURCHASING DEPARTMENTcofoe — Cofoe Medical Technology Co.,LtdSUR-FIT NATURA — CONVATEC, PURCHASING DEPARTMENTACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTNATURA+ — CONVATEC, PURCHASING DEPARTMENTACTIVELIFE — CONVATEC, PURCHASING DEPARTMENTNATURA+ — CONVATEC, PURCHASING DEPARTMENT
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-08-16 | ConvaTec, Inc | impaired functionality of the release liner |
| 2022-08-16 | ConvaTec, Inc | impaired functionality of the release liner |
| 2022-08-16 | ConvaTec, Inc | impaired functionality of the release liner |
| 2022-08-16 | ConvaTec, Inc | impaired functionality of the release liner |
| 2010-09-17 | Convatec Inc. | Mislabeled: the market units were incorrectly labeled as # 125339 ActiveLife Drainable Pouch 25 mm; the product inside was actually ActiveLife Pouch Small Tan 3 |
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