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

Recall Z-1596-2013 — Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E, QPC1721E and QFC1683E contain processing instructions, a Quick Reference Wall Chart and a flow unit. The flow unit consists of a Quick Reference Card, tubing, tethers and adapters for

U.S. FDA — Device Enforcement · United States · 2013-03-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1596-2013
Date of alert: 2013-03-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Steris Corporation
Product category: device
Product type: Devices

Reported risk: During a routine label review, the firm identified four SYSTEM 1E Quick Connects that will be updated to reflect the removal of obsolete device models. This labeling review process also highlighted the opportunity to combine two existing quick connects into a single product while eliminating the obsolete models.

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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