Bio-Signal Group Corp. recalls HydroDot Wave Prep 4 oz tubes (Product 171: Lot #29688, 31160) due to potential Burkholderia cepacia contamination. Consumers should check product details and follow official recall steps.
Product has the potential to be contaminated with Burkholderia cepacia (B. cepacia)
Bio-Signal Group Corp. is recalling HydroDot Wave Prep 4 oz tubes (Product 1710-03) because they may be contaminated with Burkholderia cepacia. This bacteria can cause infections, especially in people with weakened immune systems or medical devices.
Burkholderia cepacia is a type of bacteria that can cause serious infections in people with weakened immune systems or those using medical devices. The contamination risk comes from the product being potentially contaminated during manufacturing or handling.
People using HydroDot Wave Prep 4 oz tubes for electroconductive purposes are affected. Those with compromised immune systems or medical devices are at higher risk.
Check for HydroDot Wave Prep 4 oz tubes labeled Product 1710-03. Lot numbers 29688 and 31160 are associated with this recall.
Look for HydroDot Wave Prep 4 oz tubes with Product 1710-03 and Lot numbers 29688 or 31160.
The recall states the product may be contaminated with Burkholderia cepacia, which can cause infections. Use only if you have the specific product details and follow the recall steps.
Check the product details to see if it's affected. If it is, follow the recall steps to stop using it and contact the manufacturer.
The recall record does not mention a replacement option. Contact Bio-Signal Group Corp. for further assistance.
We’ve drafted a message you can send HydroDot to request your refund or repair — edit it as you like.
Subject: Recall Z-0704-2020 — HydroDot HydroDot Hello, I own a HydroDot that is covered by recall Z-0704-2020 from HydroDot. 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.
