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

Recall Z-0675-2016 — InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.

U.S. FDA — Device Enforcement · United States · 2016-01-05 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0675-2016
Date of alert: 2016-01-05
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Rymed Technologies, LLC
Product category: device
Product type: Devices

Reported risk: Potential for the female luer component of the InVision-Plus IV connector to crack during use.

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.

Recall Z-0675-2016 — InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products are intended for single patient use in intravenous and blood administration sets without the need for needles, thus eliminating the potential for needle-stick injuries during use.

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