Arrow recalls JACC devices with specific product codes due to potential sterility compromise from unsealed packaging. Affected units include lot numbers 13F17C0327 and 13F17F0099.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling JACC devices with Chlorag+ard Technology that may have unsealed packaging, risking sterility. This could affect medical devices used in procedures requiring sterile conditions.
The unsealed packaging could allow contamination, potentially compromising the sterility of the medical device. This risk is specific to devices used in procedures where sterility is critical, such as surgeries.
Healthcare professionals using the JACC devices for medical procedures are most at risk. Patients receiving these devices during surgery may be affected if sterility is compromised.
Check for product codes JR-42063-HPHNM or JR-42563-HPHNM. Lot numbers 13F17C0327 (for JR-42063-HPHNM) and 13F17F0099 (for JR-42563-HPHNM) indicate affected units.
Identify the product code on the device label to see if it matches JR-42063-HPHNM or JR-42563-HPHNM.
Confirm the lot number matches 13F17C0327 for JR-42063-HPHNM or 13F17F0099 for JR-42563-HPHNM.
The recall is due to potential sterility compromise from unsealed packaging, which could affect medical procedures requiring sterile conditions.
Check the product code on the device label. Affected units have codes JR-42063-HPHNM or JR-42563-HPHNM with specific lot numbers.
The recall record does not specify a remedy, so affected users should contact Arrow International for further instructions.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2015-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2015-2018 from Arrow. 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.
