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

Recall Z-2995-2018 — Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style 758000, Model CARE-E-VAC 3, Ohio Medical LLC The care-e-(R)3 is a portable medical aspirator used to suction fluids or foreign bodies from a patient. The primary intended use is to aspirate saliva, mucous, v

U.S. FDA — Device Enforcement · United States · 2018-08-14 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2995-2018
Date of alert: 2018-08-14
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Ohio Medical Corporation
Product category: device
Product type: Devices

Reported risk: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump causing an electric short leading to damage to wiring and resulting in loss of function or an inoperable unit under battery power.

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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