Use cautionMedical device recall · FDA · Published May 10, 2019
Medline Centurion Convenience Kits Recall: Risk of Over-Infusion Due to Tube Defect
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.
Take action
Contact the company
📍Recalling firmMedline Industries IncThree Lakes Drive · Northfield, IL 60093
“Medline Centurion Convenience Kits Recall: Risk of Over-Infusion Due to Tube Defect.” GovInfoNow, updated August 20, 2026. https://govinfonow.com/recall/67938-medline-centurion-convenience-kits-recall-risk-of-over-infusion-due. Based on FDA recall #Z-2067-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2067-2019%22&limit=1).
The FDA announced on 2019-05-10 that Medline Industries Inc voluntarily recalled Centurion Convenience Kits containing BD Alaris Pump Infusion Sets due to potential over-infusion of drugs, according to the FDA. The recall affects kits with specific lot codes distributed from one Illinois distributor.
The defect involves the consistency of the inner lumen thickness of the silicone tubing segment, which impacts the occlusion force necessary to fully seal the tube. This prevents the pump from complete occlusion and results in the potential for over-infusion of drug product into the patient.
Context
GovInfoNow's records show Medline Industries Inc has 48 other recalls on record since 2015-09-25. Other recent recalls include a Medline Chest Tube Kit recalled on 2022-07-21 for non-sterile tape in sterile components, a Medline Hand Sanitizer Foam recalled on 2021-11-08 for leaking containers, and a Medline Bedside PICC CDS Kit recalled on 2021-10-27 for an expired NaCl bag risk. Other recent recalls of similar products include Medline Centurion Dialysis Kits recalled on 2026-04-27 for butyrate tubing that may crack and Medline Dialysis Kits recalled on 2026-01-08 for silicone seal issues.
How to tell if you have this one
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.
Brand
Medline
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify the BD code and model numbers on the kit to confirm if it matches the recalled items.
Contact Manufacturer
Reach out to Medline Industries for guidance on next steps if you have the recalled kit.
Where it went and when
Where it was distributed
Distributed in Illinois.
Listed by the agency
Not listed
FDA distribution: “One distributor located in Illinois.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 2.3 years after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2067-2019 (May 10, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2067-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.