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

Recall Z-0526-2019 — NEOCONNECT, Enteral Extension with ENFit connector, REF EXT-60NC The NeoMed NeoConnect Enteral Only Extension Set is intended for use as an extension set for nasogastric/oralgastric or gastric tube enteral feeding tubes, incorporating safety connectors which help mitigate the risk of accidental

U.S. FDA — Device Enforcement · United States · 2018-10-24 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0526-2019
Date of alert: 2018-10-24
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Neomed Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20817584012015

Reported risk: The sterile pouch label states the expiration date is 2016-11-19, but the correct expiration date is 2019-11-09. The case label and the shipper label have the correct date

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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