Arrow recalls VPS TipTracker Stylet Access: Pouch label may not clearly show lot number or expiration date, risking confusion in catheter placement. Consumers should check for label details.
Product pouch label may not easily identify the lot number, expiration date and associated symbols..
Arrow is recalling VPS TipTracker Stylet Accessory (REF RHY-177-TTSAP) because the product pouch label might not clearly show the lot number or expiration date. This could cause confusion when using the device for catheter tip placement, potentially leading to incorrect medical procedures.
The pouch label may not easily identify the lot number, expiration date, or associated symbols. This could lead to confusion about the product's age and batch, which might affect catheter placement accuracy in medical procedures.
Medical professionals who use this accessory for central venous catheter placement may be affected. Those who rely on the label for lot number and expiration date are most at risk.
Check for the product reference number RHY-177-TTSAP on the pouch. The lot number is listed as 13F17G0074 in the recall notice.
Look for the lot number and expiration date on the pouch label to confirm if the product is affected.
The product pouch label may not easily identify the lot number, expiration date, and associated symbols, which could cause confusion in catheter placement procedures.
Check the pouch label for the lot number and expiration date. If the label is unclear, contact Arrow for guidance.
The recall addresses potential confusion in labeling, not a direct risk of injury. This is a low-risk issue.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2384-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2384-2018 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.
