Severity
Moderate
FDA Devices recall · Reported September 19, 2018
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 …
Ohio Medical Corporation recalled Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style… - a moderate-severity action.
Portable Suction Pump, (a) Style 758010, Model CARE-E-VAC 3, Ohio Medical LLC; (b) Style… was recalled by Ohio Medical Corporation in September 19, 2018. Reason: The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump c…. Check the official notice for the remedy. Verify recall #Z-2995-2018 with the FDA Devices before acting.
The recall
Ohio Medical Corporation issued this moderate-severity FDA Devices recall-The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump c….
Sourced from official FDA Devices enforcement records. Verify recall #Z-2995-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Devices action (record #Z-2995-2018) was formally reported on September 19, 2018, with the manufacturer initiating the action on August 14, 2018. It is classified under Moderate severity (Class II), with a current status of Terminated. Ohio Medical Corporation is listed as the recalling firm, operating out of Gurnee, IL. Federal records list the affected scope as 1443 units.
The documented reason for this recall is: 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 u… Distribution data in the federal record shows the product reached: US Nationwide Distribution and internationally to countries: Canada, Saudi Arabia, and United Arab Emirates.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 3 from FDA Devices - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Where this recall sits in its category - 40,322 medical devices recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Moderate
Affected scope
1443 units
Related Recalls
6
3 from same agency
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, vomitus or other aspirant from the mouth or airway to allow adequate respiration or ventilation of the patient.
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.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2995-2018 |
| Date reported | September 19, 2018 |
| Date initiated | August 14, 2018 |
| Recalling firm | Ohio Medical Corporation |
| Firm location | Gurnee, IL |
| Affected scope | 1443 units |
| Distribution | US Nationwide Distribution and internationally to countries: Canada, Saudi Arabia, and United Arab Emirates. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Devices, reported September 19, 2018. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.