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

Recall Z-0482-2022 — Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instavac I); and Instavac replacement pumps, part #AI5511, a component of model numbers 756000 and 757000.

U.S. FDA — Device Enforcement · United States · 2021-11-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0482-2022
Date of alert
2021-11-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ohio Medical Corporation
Product category
device
Product type
Devices
Reported risk: Increase in premature device failures
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.

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