Use cautionMedical device recall · FDA · Published October 17, 2025
BD Alaris Infusion Pump Module 8100 Recall: Drop or Jar Risk
Recall of BD Alaris infusion pump modules 8100 and related parts due to risk of under/over-infusion if dropped or jarred. Affected units sold after June 19, 2004.
If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump module failure to calibrate; so dropped/jarred pumps should be removed from use, tested, and inspected by qualified service personnel prior to reuse; tip sheet, cleaning and disinfecting procedure and reference guide updated.
Take action
Contact the company
📍Recalling firmCareFusion 303, Inc.10020 Pacific Mesa Blvd · San Diego, CA 92121-4386
✎ GovInfoNow plain-language explainer
CareFusion recalls BD Alaris infusion pump modules 8100 and related parts because dropping or jarring them can cause damage that leads to incorrect medication delivery. Affected units were sold after June 19, 2004 and must be checked by a qualified technician before reuse. Read more at govinfonow.com/recall/51045-bd-alaris-infusion-pump-module-8100-recall-drop-or-jar.
“BD Alaris Infusion Pump Module 8100 Recall: Drop or Jar Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/51045-bd-alaris-infusion-pump-module-8100-recall-drop-or-jar. Based on FDA recall #Z-0430-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0430-2026%22&limit=1).
The FDA announced on Oct. 17, 2025, that CareFusion 303, Inc. is recalling BD Alaris infusion Pump Module 8100 and related bezel assemblies due to potential under- or over-infusion if the device is dropped. The agency classified the recall as Class I.
How to tell if you have it
BD Alaris infusion Pump Module 8100, REF: 8100
KIT, BEZEL ASSY 8100BD, REF: 49000437
KIT ASSY ONE PIECE BEZEL 8100, REF: 49000270
The hazard
If the infusion pump is dropped or severely jarred, it may damage the pump module bezel assembly. This damage can cause under-infusion, over-infusion, unregulated flow, or pump module failure to calibrate.
Context
GovInfoNow's records show CareFusion 303, Inc. has 64 other recalls on record since 2017-06-12. Other recent recalls include the BD Pyxis MedStation 403 Medication Cabinet Recall (2026-04-30), the CareFusion TLS version labeling recall (2026-02-11), and the BD Pyxis ES Enterprise Server Software Update Issue Recall (2025-12-03). Other recent recalls of similar products include the BD Alaris Pump Infusion Sets Recall (2026-08-19), the Fresenius Kabi LVP-0004 Infusion Pump Recall (2026-02-04), and the Medtronic MiniMed 780G Insulin Pump Recall (2026-07-13).
How to tell if you have this one
Check for the model numbers 8100, 49000437, or 49000270 on the pump module. Units sold after June 19, 2004 are affected. The reference codes listed in the recall include specific serial numbers.
Brand
BD Alaris
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Pump Module
Inspect the pump module for any signs of damage or previous drops/jarring.
Get Professional Inspection
Have a qualified service technician test and inspect the pump module before reuse.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide distribution. US nationwide including Puerto Rico, Guam, American Samoa, Northern Mariana Islands; and countries of SG, BH, AE, JP, CA, IT, QA, PH, DE, TW, PK, KR, BW, SA, MY, IL, NZ, AU, IN, GB, CN, NL, FR, ZA, BE, MX, CH, GI,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
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-0430-2026 (October 17, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0430-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.