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

Recall Z-2365-2016 — Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed one per carton. The lnvacare Precise Rx" Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the primary source for moni

U.S. FDA — Device Enforcement · United States · 2016-06-21 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2365-2016
Date of alert: 2016-06-21
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Invacare Corporation
Product category: device
Product type: Devices

Reported risk: The rear gradation scale was screen printed upside down on the flowmeter gauge.

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.

Related