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

Recall Z-1873-2017 — Laerdal Compact Suction Unit ¿ 4 under the following labels: 1) 300 ml (3.3 lbs) canister version - CATALOG #(s): 88006101 - LCSU 4, 300 ml Complete unit (US), 88006103 - LCSU 4, 300 ml Complete unit (UK), 88006140 - LCSU 4, 300 ml Complete unit (EUR), 881151 - Replacement unit, 88006201 - LCSU 4, 3

U.S. FDA — Device Enforcement · United States · 2017-01-08 · 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-1873-2017
Date of alert: 2017-01-08
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Laerdal Medical Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20150501

Reported risk: The On/Off functionality in the LCSU 4 is controlled by electronic components, one of which might be damaged.

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