Arrow International recalls VPS Rhythm ECG Accessory Packs with Johans Adapter due to potential sterility compromise from unsealed packaging. Affected units include specific product codes and lot numbers.
Product sterility may be compromised due to unsealed packaging.
Arrow International is recalling VPS Rhythm ECG Accessory Packs with Johans Adapter because the packaging may not be sealed properly, risking contamination. This could lead to infections if the device is used without proper sterility.
The packaging may not be sealed properly, which could allow contamination. If the device is used without proper sterility, it might lead to infections or other health issues.
Users of the VPS Rhythm ECG Accessory Pack with Johans Adapter are affected. Healthcare professionals and individuals using medical devices for monitoring are most at risk.
Check for product codes RHY-100-ECGJ and lot numbers 13F17A0120, 13F17A0287, 13F17C0018, 13F17D0136, or 13F17E0122. The product was sold by Arrow International.
Verify your product code and lot number against the listed codes and lot numbers to confirm if it is affected.
The recall states that the packaging may not be sealed properly, which could compromise sterility. If you have the affected product, it is recommended to check the recall details.
The recall does not specify a remedy, so you should check the product details to see if it is affected and contact Arrow International for further instructions.
Check for product codes RHY-100-ECGJ and lot numbers 13F17A0120, 13F17A0287, 13F17C0018, 13F17D0136, or 13F17E0122.
We’ve drafted a message you can send Arrow International to request your refund or repair — edit it as you like.
Subject: Recall Z-2026-2018 — Arrow International Arrow International Hello, I own a Arrow International that is covered by recall Z-2026-2018 from Arrow International. 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.
