Home › CONVATEC, PURCHASING DEPARTMENT › ACTIVELIFE
ACTIVELIFE
CONVATEC, PURCHASING DEPARTMENT · Model 125359 · UDI-DI 00768455102136
EZQ
Prescription
6
510(k) clearances
2,020
Adverse events (1 deaths)
5
Recalls
49
Facilities
Description
ACTIVELIFE Convex One-Piece Pre-Cut Drainable Pouch with Durahesive Skin Barrier, with 1 Sided Comfort Panel with Tape 12 in, Trans, 1 3/4 in
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 32 mm, ICC # 125333. |
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 docsData 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.
