Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported July 18, 2018
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facility as a means to evacuate media (i.e. fluids) from the body.
Final quality control testing was not completed before the devices were distributed..
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Ohio Medical Corporation recalled Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The … - a moderate-severity action.
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The … was recalled by Ohio Medical Corporation in July 18, 2018. Reason: Final quality control testing was not completed before the devices were distributed... Check the official notice for the remedy. Verify recall #Z-2410-2018 with the FDA Devices before acting.
The recall
Ohio Medical Corporation issued this moderate-severity FDA Devices recall-Final quality control testing was not completed before the devices were distributed...
- Moderate
- severity level
- 11 units
- affected scope
- Class II
- classification
- July 18, 2018
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2410-2018 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2410-2018) was formally reported on July 18, 2018, with the manufacturer initiating the action on March 12, 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 11 units.
The documented reason for this recall is: Final quality control testing was not completed before the devices were distributed.. Distribution data in the federal record shows the product reached: US Nationwide Distribution in the states of NC, IN, TN, LA,, FL MI, IL.. 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 - 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.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 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.
Affected scope
11 units
Related Recalls
6
0 from same agency
Product description
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facility as a means to evacuate media (i.e. fluids) from the body.
Reason for recall
Final quality control testing was not completed before the devices were distributed..
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2410-2018 |
| Date reported | July 18, 2018 |
| Date initiated | March 12, 2018 |
| Recalling firm | Ohio Medical Corporation |
| Firm location | Gurnee, IL |
| Affected scope | 11 units |
| Distribution | US Nationwide Distribution in the states of NC, IN, TN, LA,, FL MI, IL. |
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.
- Check the recall number (Z-2410-2018) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
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.
Frequently Asked Questions
What product was recalled? ▼
Vacuum Regulator, Push-T-Set Intermittent Suction Unit (PTS-ISU) Product Usage: The vacuum regulator is intended to be used in a medical facility as a means to evacuate media (i.e. fluids) from the body.. Recalled by Ohio Medical Corporation. Units affected: 11 units.
Why was this product recalled? ▼
Final quality control testing was not completed before the devices were distributed..
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 18, 2018. Severity: Moderate. Recall number: Z-2410-2018.
Where was the recalled product distributed? ▼
Distribution: US Nationwide Distribution in the states of NC, IN, TN, LA,, FL MI, IL..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2410-2018) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
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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 July 18, 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.