Ohio Medical Corporation recalls vacuum regulators for incomplete quality control testing. Affected units have specific model numbers and lot numbers. Consumers should contact the company for details.
Final quality control testing was not completed before the devices were distributed..
Ohio Medical Corporation is recalling vacuum regulators used in medical facilities. The recall is due to incomplete final quality control testing before distribution, which could lead to improper function in critical medical use.
The vacuum regulator was distributed without completing final quality control testing. This could result in improper evacuation of fluids from patients if the device malfunctions during medical procedures.
Medical facilities using the vacuum regulator for patient suction. Staff handling the device are most at risk if it fails during critical procedures.
Check for model numbers 8702-1251-908, 8701-1251-901, 8705-1251-907, 8701-1251-908, 8705-1251-901. Also look for lot number ISU177359 or device unit numbers listed in the recall notice.
Reach out to Ohio Medical Corporation for specific instructions on how to verify your unit and get replacement or repair options.
The recall is due to incomplete final quality control testing before distribution, which could lead to improper function in critical medical use.
Affected model numbers include 8702-1251-908, 8701-1251-901, 8705-1251-907, 8701-1251-908, and 8705-1251-901.
Check for lot number ISU177359 or device unit numbers listed in the recall notice, such as JGGW24156, JGGW24193, and others.
We’ve drafted a message you can send Ohio Medical Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-2410-2018 — Ohio Medical Corporation Ohio Medical Corporation Hello, I own a Ohio Medical Corporation that is covered by recall Z-2410-2018 from Ohio Medical Corporation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
