Arrow recalls AGB+ Multi-Lumen CVC Kits (CDC-45703-1A) due to potential allergic reactions in patients sensitive to chlorohexidine, silver sulfadiazine, or sulfa. Affected kits may have incorrect labeling.
The lidstock / information card on the kits correctly states the product code as CDC-45703-1A. The banner card on the side of the kit may incorrectly state the product code as CDC-15703-1A and not identify the product as a coated ARROWg+ard Blue PLUS (AGB+) antimicrobial catheter which may cause a minor delay during use and placement of a coated catheter in patients with known sensitivity to chlorohexidine, silver sulfadiazine or sulfa could result in an allergic reaction
Arrow is recalling its AGB+ Multi-Lumen CVC Kits (product code CDC-45703-1A) because some kits might incorrectly label the product as CDC-15703-1A, which could cause allergic reactions in patients sensitive to certain chemicals. This means the kits might not be safe for people with known allergies to chlorohexidine, silver sulfadiazine, or sulfa.
The kits may have incorrect labeling that fails to identify the product as a coated ARROWg+ard Blue PLUS (AGB+) antimicrobial catheter. This could lead to allergic reactions in patients with known sensitivities to chlorohexidine, silver sulfadiazine, or sulfa.
Patients receiving central venous catheter procedures using the recalled kits are at risk, particularly those with known sensitivities to chlorohexidine, silver sulfadiazine, or sulfa. Healthcare providers using the kits should check the product code.
Check the product code on the lidstock or information card; the correct code is CDC-45703-1A. Kits with the incorrect code CDC-15703-1A on the banner card may be affected.
Look for the product code CDC-45703-1A on the lidstock or information card to confirm it is not the incorrect CDC-15703-1A.
The recall is due to potential incorrect labeling that could cause allergic reactions in patients sensitive to chlorohexidine, silver sulfadiazine, or sulfa.
The correct product code is CDC-45703-1A as stated on the lidstock or information card.
The recall record does not specify a remedy, so no action is required beyond checking the product code.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-1106-2021 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-1106-2021 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.
