Product Wiki · Recalls · U.S. FDA — Device Enforcement

Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660, t) 423661 — recall Z-1350-2024

U.S. FDA — Device Enforcement · United States · 2024-02-19 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1350-2024
Date of alert: 2024-02-19
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ConvaTec, Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 768455203925

Reported risk: Convatec Inc is conducting a Voluntary Medical Device Recall (removal) for specific lots of the EsteemBody Soft Convex, Drainable Pouch due to inconsistency in the strength of the filter weld.

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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