National Distribution & Contracting Inc recalls ECO 50TS Gel Tens Ultrasound devices due to potential bacterial contamination in ultrasound gels. Consumers should check product codes and contact the company for details.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
National Distribution & Contracting Inc is recalling ECO 50TS Gel Tens Ultrasound devices because ultrasound gels may contain bacteria. This could lead to infections if the product is used without proper cleaning.
The ultrasound gels and lotions could have bacterial contamination. If the gel is used without proper cleaning, it might cause infections. This is a potential health risk but not an immediate danger.
Users of ECO 50TS Gel Tens Ultrasound devices who purchased the product from the manufacturer. People with compromised immune systems may be at higher risk.
Check for the product code ECO 50TS on the device. The product was sold with the description 'Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl'.
Look for the product code ECO 50TS on the device to confirm if it is recalled.
The recall states that ultrasound gels may contain bacterial contamination, so it is not recommended for use without proper cleaning.
Check for the product code ECO 50TS on the device. The product was sold with the description 'Gel Tens Ultrasound 1in X 5L cube 1 Dispenser Btl'.
The recall does not specify a remedy, so contact National Distribution & Contracting Inc for further instructions.
We’ve drafted a message you can send National Distribution & Contracting Inc to request your refund or repair — edit it as you like.
Subject: Recall Z-0068-2022 — National Distribution & Contracting Inc National Distribution & Contracting Inc Hello, I own a National Distribution & Contracting Inc that is covered by recall Z-0068-2022 from National Distribution & Contracting Inc. 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.
