Arrow recalls 0.2 micron flat epidural filters (product code EF-05500) due to potential sterility compromise from unsealed packaging. Affected lot numbers include 13F17D0240, 13F17G0371, and 13F17K0408.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling 0.2 micron flat epidural filters with product code EF-05500 because the packaging may not be sealed properly, risking contamination. This could lead to infections or other complications during medical procedures.
The filters' packaging may not be sealed, which could allow contamination. This poses a risk of infection or other complications during medical procedures if the filters are used without proper sterility.
Healthcare professionals using the filters for epidural procedures are most at risk. Patients receiving these filters during surgery may be affected if the filters become contaminated.
Check for product code EF-05500 on the filter packaging. Affected lot numbers are 13F17D0240, 13F17G0371, and 13F17K0408.
Inspect the packaging for signs of being unsealed or damaged.
The product code is EF-05500.
Affected lot numbers are 13F17D0240, 13F17G0371, and 13F17K0408.
Check for product code EF-05500 and affected lot numbers on the packaging.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2013-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2013-2018 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.
