Alaris Pump Module
Medical device recall Z-0026-2018. Published in FDA’s Enforcement Report on Oct 25, 2017.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Oct 25, 2017. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Ongoing its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 31,622 units (28,224 in US) how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
The recalling firm has received reports of increased or decreased flows that have occurred in certain pumps.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Alaris Pump Module model 8100 manufactured between November 2011 and March 2012; Alaris Pump Module serviced with LVP Mechanism Sub Assembly (P/N) 10942012 between November 2011 and March 2012; Alaris Pump module Bezel Kit Assembly (P/N) 10964559) shipped between November 2011 and March 2012. The Alaris Pump module is a large volume infusion pump offered under the Alaris System. The Alaris Pump module will deliver medication and fluids using the IV administration sets for continuous or intermittent delivery through clinically acceptable routes of administration such as intravenous or epidural.
31,622 units (28,224 in US), in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
All Alaris Pump module model 8100 manufactured and serviced with the bezel assembly manufactured between October 2011 and November 2011; Serial Numbers - Serial 13537720 13537735 13538005 13538811 13540340 13541935 13543108 13543503…
Every code shown here, 1,995 characters
All Alaris Pump module model 8100 manufactured and serviced with the bezel assembly manufactured between October 2011 and November 2011; Serial Numbers - Serial 13537720 13537735 13538005 13538811 13540340 13541935 13543108 13543503 13543666 13544201 13544350 13545092 13545892 13546315 13546638 13548091 13550608 13550614 13550629 13550670 13552666 13552667 13552781 13552782 13553628 13553661 13553714 13553730 13553739 13554035 12851369 12851850 9879510 9879561 9880323 9880838 9881158 12564799 13157405 13563286 13566911 13566932 13566933 13567118 13585121 13585213 13585493 13586248 13586314 13586329 13586339 13586340 13586408 13586578 13586723 13586731 13586733 13586738 13586746 13586758 13586763 13586764 13586768 13586775 13586782 13586784 13586793 13586795 13586797 13586798 13586819 13586820 13586835 13586836 13586839 13586855 13586860 13586877 13586878 13586898 13586952 13586957 13586960 13586967 13586976 13587076 13587077 13587118 13587220 13587231 13587232 13587233 13587262 13587263 13587266 13587289 13587290 13587291 13587297 13587312 13587315 13587345 13587398 13196293 13203541 13207333 13213463 13214795 13217554 13219137 13219971 13375015 13375617 13375737 12471635 9857470 9858862 9858865 9859690 9860106 9860746 13184877 13186091 13582527 13582709 13599442 12460530 12474814 12771113 13619912 13620162 13585671 13566067 13616956 13545222 13545224 13545250 13545260 13545262 13550278 13550317 13550318 13550319 13550325 13550337 13550365 13550369 13550370 13550379 13553239 13549816 13549832 13549886 13549901 13549903 13550267 13550271 13550339 13550340 13550345 13550346 13550355 13550356 13550357 13550366 13553126 13553134 13553403 13553415 13568914 13568950 13569155 13569179 13569248 13569694 13569829 13569830 13569838 13569839 13569854 13569876 13569947 13569948 13569953 13569955 13569957 13570013 13570014 13570015 13570017 13570022 13570023 13570052 13570063 13570076 13570077 13570127 13570128 13570137 13570138 13570168 13570184 13570198 13570222 13570236…
FDA’s list runs to 278,670 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Worldwide Distribution - USA (nationwide) and to the countries of : Canada, Australia, UAE, Kuwait, Saudi Arabia, South Africa
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Ongoing, in FDA’s file.
“A recall which is currently in progress.”
openFDA, on “On-Going”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Aug 9, 2017.
- FDA classified it on Oct 19, 2017.
- FDA’s Enforcement Report published it on Oct 25, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- CareFusion 303, Inc., of San Diego, CA.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 278,670 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.