Arrow recalls single-lumen catheter kits with unsealed packaging that may compromise sterility. Affected products include specific model codes and lot numbers from 2013.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling single-lumen central venous catheterization kits because the packaging might not be sealed properly, risking contamination. This could lead to infections if the kit is used without proper sterility.
The packaging may not seal correctly, allowing contaminants to enter the kit. This could lead to infections during medical procedures if the kit is used without proper sterility checks.
Healthcare professionals using these kits for medical procedures are most at risk. Patients receiving treatments with the recalled kits could face infection if the packaging was compromised.
Check for model codes ASK-04301-TJ and lot numbers 13F17E0674, 13F17G0265, 13F17J0087, 13F17K0099, or 13F17L0250. These kits were sold with specific packaging that may not seal properly.
Inspect the packaging for signs of being unsealed or damaged before use.
The packaging may not seal properly, risking contamination and infection during medical procedures.
Model codes ASK-04301-TJ with lot numbers 13F17E0674, 13F17G0265, 13F17J0087, 13F17K0099, and 13F17L0250.
No specific stop-use instruction is given; check the packaging seal before use.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1974-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1974-2018 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.
