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

Recall Z-2632-2017 — 3M Ranger(TM) Pressure Infusor, Model 145, SKU 70200792979 The 3M Ranger Pressure Infusor is a hardware device intended to provide pressure to I.V. solution bags when rapid infusion of liquids is required.

U.S. FDA — Device Enforcement · United States · 2017-05-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2632-2017
Date of alert: 2017-05-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: 3M Company - Health Care Business
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 70200792979

Reported risk: It was discovered that one Ranger Pressure lnfusor Model 145, SN: 100873, produced a left chamber pressure that was slightly below the manufacturing specification.

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

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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.

Recall Z-2632-2017 — 3M Ranger(TM) Pressure Infusor, Model 145, SKU 70200792979 The 3M Ranger Pressure Infusor is a hardware device intended to provide pressure to I.V. solution bags when rapid infusion of liquids is required.

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