Arrow recalls Peripherally Inserted Midline Catheter Kit with Placement Wire (REF MK-02031-TW) due to pouch label not clearly showing lot number, expiration date, or symbols. This may cause confusion during catheter use.
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Arrow is recalling a Peripher: Inserted Midline Catheter Kit with Placement Wire (REF MK-02031-TW) because the product pouch label may not clearly show the lot number, expiration date, or symbols. This could lead to confusion when using the catheter.
The pouch label may not clearly show the lot number, expiration date, or symbols. This could cause confusion when verifying the catheter's details during medical procedures, but does not pose a direct safety risk.
Healthcare professionals who use this catheter kit for real-time tip location monitoring may be affected. Patients receiving this catheter treatment are at low risk if the label issue is corrected.
Check for the product reference number MK-02031-TW on the pouch. The lot number is 13F16M0102, but the label may not clearly display this information.
Look for the lot number, expiration date, and symbols on the pouch label to confirm the product details.
The pouch label may not clearly show the lot number, expiration date, or symbols, which could cause confusion during catheter use.
Check the pouch label for the lot number, expiration date, and symbols. If the label is unclear, contact Arrow for assistance.
This recall is low risk as it only affects label clarity, not the safety of the catheter itself.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2385-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2385-2018 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.
