Arrow recalls PI Midline 2L catheters (CDC-32052-MPKC) due to potential contamination in medication kits, 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 PI Midline 2L catheters because medication kits included in the product may have been contaminated, risking serious or life-threatening injuries if the sterility of the medication is compromised.
The medication kits (containing lidocaine, bupivacaine, and saline) may have been contaminated by the supplier, which could compromise the sterility of the injectable product. If the medication is not sterile, it could lead to serious or life-threatening infections or injuries.
Healthcare professionals using the PI Midline 2L catheters for medical procedures are most at risk. Patients receiving injections through these catheters could also be affected if the medication is contaminated.
Check for the product code CDC-32052-MPKC on the catheter packaging. The lot number 10801902193275 and batch code 33F24L0236 are also associated with this recall.
Immediately stop using the PI Midline 2L catheters with the product code CDC-32052-MPKC if you have them.
The supplier of the medication kits had quality issues, which could lead to contaminated medication and serious or life-threatening injuries if the sterility is compromised.
Stop using the PI Midline 2L catheters with the product code CDC-32052-MPKC immediately and contact Arrow for further instructions.
The recall is active immediately; there is no specific deadline for action.
We’ve drafted a message you can send Arrow to request your refund or repair — edit it as you like.
Subject: Recall Z-2387-2026 — Arrow Arrow Hello, I own a Arrow that is covered by recall Z-2387-2026 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.
