Arrow recalls Pressure Injectable ARROWg+ard Blue PLUS MultiLumen Central Venous Catheterization Kits with incorrect Springwire Guide (SWG) that could cause improper use during medical procedures.
These finished good kits may contain the incorrect Springwire Guide (SWG).
Arrow is recalling specific pressure injectable catheter kits that may contain the wrong Springwire Guide. This could lead to improper use during medical procedures if the kit is used without the correct guide.
The kits may contain the incorrect Springwire Guide (SWG) which could lead to improper use during medical procedures. This might cause complications if the catheter is not properly positioned or secured.
Healthcare professionals using the recalled catheter kits are most at risk. Patients receiving procedures with these kits could be affected if the incorrect guide causes improper use.
Check for product codes ASK-45703-PNHS, ASK-45703-PGMCL, or ASK-45703-PNW with expiration dates from February 2018 to November 2018. Lot numbers include 23F16M0498, 23F17A0505, or 23F17B0116.
Verify the product code on the kit to see if it matches ASK-45703-PNHS, ASK-45703-PGMCL, or ASK-45703-PNW.
The kits may contain the incorrect Springwire Guide (SWG) which could lead to improper use during medical procedures.
Check for product codes ASK-45703-PNHS, ASK-45703-PGMCL, or ASK-45703-PNW with expiration dates from February 2018 to November 2018 and lot numbers 23F16M0498, 23F17A0505, or 23F17B0116.
The recall does not specify a stop-use instruction, so you can continue using them but should check if they match the recalled product codes.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0649-2018 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0649-2018 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.
