Arrow recalls certain PICC kits due to potential sterility issues in injectable products, which could lead to serious or life-threatening injuries. Affected kits include specific models and batch numbers.
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 specific PICC (peripherally inserted central catheter) kits because a supplier had quality issues with the lidocaine, bupivacaine, and saline solutions inside them. If the sterility of these injectable products is compromised, it could cause serious or life-threatening injuries.
The supplier used in this recall had quality issues with the lidocaine, bupivacaine, and 0.9% sodium chloride solutions. If the sterility of these injectable products is compromised, it could lead to serious or life-threatening injuries such as infections or other complications.
Patients using these PICC kits for medical procedures are most at risk, particularly those who have received the recalled kits from Arrow. Healthcare providers who use these kits in medical settings may also be affected.
Check the product labels for specific model numbers like DLX-35563-HPKC, ASK-44552-ABKB, or CDC-45552-VPS2. Also look for batch numbers such as 10801902193275 or 33F25D0520.
Look for model numbers like DLX-35563-HPKC, ASK-44552-ABKB, or CDC-45552-VPS2 on the kit packaging.
A supplier had quality issues with the lidocaine, bupivacaine, and 0.9% sodium chloride solutions in these kits, which could lead to serious or life-threatening injuries if sterility is compromised.
Check the product labels for the model numbers and batch numbers listed in the recall notice. If you have the recalled kits, contact Arrow for further instructions.
If the sterility of the injectable products is compromised, it could cause serious or life-threatening injuries such as infections or other complications.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2378-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2378-2026 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.
