Medline recalls Centurion Convenience Kits with BD Alaris Pump Infusion Sets (BD code 11522558) due to silicone tubing defects that may cause over-infusion of medication. Affected kits include specific model numbers and production lots.
This recall is a sub recall to BD s recent Class I recall for the Alaris Pump Infusion Set due to an issue with the consistency of the inner lumen thickness of the silicone tubing segment which directly impacts amount of occlusion force necessary to fully seal the tube. This defect prevents the pump from complete occlusion and results in the potential for over-infusion of drug product into the patient.
Medline is recalling Centurion Convenience Kits that contain BD Alaris Pump Infusion Sets because a defect in the silicone tubing can cause over-infusion of medication. This risk could lead to serious harm if the pump fails to seal properly.
The silicone tubing has inconsistent thickness, which prevents the pump from sealing properly. This defect can cause the pump to over-infuse medication into the patient, potentially leading to serious harm.
Adults, children, and neonates using the Centurion Convenience Kits with BD Alaris Pump Infusion Sets. Patients receiving medical infusions are most at risk if the kit is used without the fix.
Check for BD code 11522558 (Centurion code 110931) inside kits labeled DYNJ52509A or DYNJ52510A. Affected products were sold with production lots from 2018090590 through 2019040190.
Identify the BD code and model numbers on the kit to confirm if it matches the recalled items.
Reach out to Medline Industries for guidance on next steps if you have the recalled kit.
The silicone tubing has inconsistent thickness, which can prevent the pump from sealing properly and cause over-infusion of medication.
Kits labeled DYNJ52509A or DYNJ52510A with BD code 11522558 (Centurion code 110931).
Yes, the defect may cause over-infusion of medication, which could lead to serious harm if the pump fails to seal properly.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2067-2019 — Medline Medline Hello, I own a Medline that is covered by recall Z-2067-2019 from Medline. 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.
