Inter-Med recalls 6% sodium hypochlorite dental syringes with potential degraded rubber bung that could leak bleach. Affected lots include 2018-1348 to 20190835. Stop using immediately to avoid chemical exposure.
The affected lots may be packaged in syringes which include an incorrect bung. The incorrect bung is made of a latex-free isoprene rubber material. After prolonged storage and exposure to contained solutions, the rubber bung may degrade due to chemical interaction with the bleach solution.
Inter-Med is recalling dental bleach syringes that may have a degraded rubber bung causing leaks. This could lead to chemical exposure if the syringe is used improperly. Owners should stop using these syringes to prevent potential injury.
The syringe's rubber bung may degrade over time due to chemical interaction with the bleach solution. This degradation could cause leaks, potentially leading to chemical exposure if the syringe is used.
Dental professionals and patients using the recalled syringes for cleaning. Those who have the specific lot numbers listed are most at risk.
Check for lot numbers 2018-1348, 2018-1585, 2018-1586, 2018-1852, 20182106, 20182302, 20182458, 20190725, or 20190835 on the syringe packaging. The product is labeled as Vista Dental Products Sodium Hypochlorite - 6%, 10-12cc Pre-filled Syringes.
Look for the lot numbers listed in the recall: 2018-1348, 2018-1585, 2018-1586, 2018-1852, 20182106, 20182302, 20182458, 20190725, or 20190835.
If you have a recalled syringe, stop using it to prevent potential chemical exposure from leaks.
The rubber bung may degrade over time due to chemical interaction with the bleach solution, potentially causing leaks.
Check for lot numbers 2018-1348, 2018-1585, 2018-1586, 2018-1852, 20182106, 20182302, 20182458, 20190725, or 20190835 on the syringe packaging.
The recall record does not specify a return process or remedy.
We’ve drafted a message you can send Inter-Med to request your refund or repair — edit it as you like.
Subject: Recall Z-0012-2020 — Inter-Med Inter-Med Hello, I own a Inter-Med that is covered by recall Z-0012-2020 from Inter-Med. 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.
