Arrow recalls MAC Two-Lumen Central Venous Access Kits with potential for inadequate connection between Micro Clave Clear Connectors and Arrowg+ard Blue Plus Three-Lumen CVC Kits, causing possible complications.
There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.
Arrow is recalling a specific central venous access kit that may not connect properly with another Arrow product, potentially causing complications. This affects medical devices used for catheter placements in hospitals and clinics.
The Micro Clave Clear Connectors in the kit may not connect securely with the Arrowg+ard Blue Plus Three-Lumen CVC Kit, potentially leading to leaks or disconnections during medical procedures. This could cause complications like infection or improper catheter placement.
Healthcare professionals using the Arrow MAC Two-Lumen Central Venous Access Kit with 7-7.5 Fr catheters are most at risk. Patients receiving these devices during medical procedures could be affected.
Check for the product name 'Arrow MAC Two-Lumen Central Venous Access Kit' with reference number ASK-11242-UPM1. The kit was sold with lot number 13F22C0349 and UDI/DI 10801902159448.
Verify the product reference number ASK-11242-UPM1 and lot number 13F22C0349 on the kit.
The recall states there is a potential for inadequate connection between components, which could lead to complications, but the exact risk level is not specified.
The recall record does not specify a remedy, so no action is required at this time.
Look for the product reference number ASK-11242-UPM1 and lot number 13F22C0349 on the kit.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-0351-2023 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-0351-2023 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.
