Arrow recalls catheter hemostasis valves with unsealed packaging that may compromise sterility. Product code AI-07000, lot numbers 13F17C0232-13F17J0083. Stop using if unsealed.
Product sterility may be compromised due to unsealed packaging.
Arrow is recalling catheter hemostasis valves that may have unsealed packaging, risking sterility. This could lead to infections during medical procedures if the valve is used without proper sterility.
The valve packaging may not be sealed properly, allowing contamination. This could lead to infections during medical procedures if the valve is used without proper sterility.
Healthcare professionals using the catheter hemostasis valve for medical procedures. Patients receiving procedures with this valve are at risk if sterility is compromised.
Check for product code AI-07000 and lot numbers 13F17C0232, 13F17G0194, 13F17H0047, or 13F17J0083. The valve is used with guide wires 0.038 inches (0.096 cm) or smaller.
Inspect the packaging for any signs of being unsealed or damaged.
The packaging may not be sealed properly, risking contamination and potential infection during medical procedures.
Product code AI-07000.
Lot numbers 13F17C0232, 13F17G0194, 13F17H0047, and 13F17J0083.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1957-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1957-2018 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.
