Arrow recalls specific PICC kits due to potential contamination of lidocaine, bupivacaine, and saline solutions which could cause serious or life-threatening injuries if sterility is compromised.
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Arrow is recalling certain PICC (peripherally inserted central catheter) kits because they may contain contaminated medication. If the sterility of the water-based injectable products is compromised, users could face serious or life-threatening injuries.
The supplier of the medication in these kits had quality issues, which could lead to contamination. If the sterility of the water-based injectable products is compromised, this might cause serious or life-threatening injuries.
Healthcare professionals and patients who use the recalled PICC kits for medical procedures are at risk. Those who have the specific model numbers listed in the recall are most vulnerable.
Check for the model numbers listed in the recall: ASK-44063-NS, ASK-45052-NS, ASK-45541-MHBV, ASK-45552-RH, and other specific codes. These kits were sold with batch numbers starting with 10801902193275.
Discontinue use of all recalled PICC kits as they may contain contaminated medication that could cause serious or life-threatening injuries.
Arrow is recalling specific PICC kits with model numbers including ASK-44063-NS, ASK-45052-NS, and others, as listed in the recall notice.
Check the model number on the kit, which should be one of the specific codes listed in the recall, such as ASK-44063-NS or ASK-45052-NS, and the batch number starting with 10801902193275.
Immediately stop using the kit and contact Arrow for further instructions. The recall is for safety due to potential contamination of medication.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2370-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2370-2026 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.
