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

Recall Z-0195-2023 — Y-CONNECTOR: 6" Small Kink Resistant Tubing Bifurcated Connector /2 Male Luer Locks, 1 Female Luer Lock, Labeled as: SUMMIT MEDICAL PRODUCTS, REF 220227; MPS Acacia CAT NO: BC-006-04; MEDICAL PRODUCTS SPECIALISTS EXTENSION SET, Catalog Number BC00604, pain control pump accessory

U.S. FDA — Device Enforcement · United States · 2022-09-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0195-2023
Date of alert
2022-09-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Avanos Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Sterile extension sets were distributed without an expiration 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.

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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.