Instavac Portable Suction Pump, Constant mode (model #757000, Instavac C) and Intermittent mode (model 756000, Instav... — FDA record Z-0482-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 16, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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.
Reason
Increase in premature device failures
Classification
Class II
Recalling firm
Ohio Medical Corporation
Quantity
649 portable suction pumps and replacement pumps
Agency-reported status
Ongoing
Source record identifier
Z-0482-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityShipped between March 2019 and February 2021.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide, including PR. There was government and foreign distribution. There was no military distribution.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jan 19, 2022
Recall initiation date
Nov 16, 2021
Center classification date
Jan 11, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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