The Patient Control Module (PCM) is used in conjunction with a Baxter infusor as a single use device for the…
Medical device recall Z-1536-2015. Published in FDA’s Enforcement Report on May 6, 2015.
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 May 6, 2015. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Florida the one state its words name
- 7,596 patient control modules 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?
Potential for device malfunction resulting in flow when the device should not be flowing
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
The Patient Control Module (PCM) is used in conjunction with a Baxter infusor as a single use device for the control of intermittent bolus doses of medication based on patient demand.
7,596 patient control modules, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
1) Product Code: 2C1067; Lots and Expiration Dates: Lot 11D001 , Expires 4/1/2014 ; Lot 11D068 , Expires 4/1/2014 ; Lot 11E048 , Expires 5/1/2014 ; Lot 11E084 , Expires 5/1/2014 ; Lot 11F050 , Expires 6/1/2014 ; Lot 11G019 , Expires…
Every code shown here, 1,998 characters
1) Product Code: 2C1067; Lots and Expiration Dates: Lot 11D001 , Expires 4/1/2014 ; Lot 11D068 , Expires 4/1/2014 ; Lot 11E048 , Expires 5/1/2014 ; Lot 11E084 , Expires 5/1/2014 ; Lot 11F050 , Expires 6/1/2014 ; Lot 11G019 , Expires 7/1/2014 ; Lot 11H019 , Expires 8/1/2014 ; Lot 11H074 , Expires 8/1/2014 ; Lot 11J042 , Expires 9/1/2014 ; Lot 11J078 , Expires 9/1/2014 ; Lot 11M078 , Expires 11/1/2014 ; Lot 11N027 , Expires 12/1/2014 ; Lot 12A020 , Expires 1/1/2015 ; Lot 12A037 , Expires 1/1/2015 ; Lot 12A050 , Expires 1/1/2015 ; Lot 12A095 , Expires 2/1/2015 ; Lot 12B040 , Expires 2/1/2015 ; Lot 12C033 , Expires 3/1/2015 ; Lot 12D016 , Expires 4/1/2015 ; Lot 12D041 , Expires 4/1/2015 ; Lot 12D089 , Expires 4/1/2015 ; Lot 12E004 , Expires 5/1/2015 ; Lot 12F010 , Expires 6/1/2015 ; Lot 12F036 , Expires 6/1/2015 ; Lot 12G032 , Expires 7/1/2015 ; Lot 12G034 , Expires 7/1/2015 ; Lot 12G057 , Expires 7/1/2015 ; Lot 12H012 , Expires 7/1/2015 ; Lot 12H033 , Expires 8/1/2015 ; Lot 12H077 , Expires 8/1/2015 ; Lot 12J047 , Expires 9/1/2015 ; Lot 12K008 , Expires 10/1/2015 ; Lot 12M036 , Expires 11/1/2015 ; Lot 12N031 , Expires 12/1/2015 ; Lot 13A016 , Expires 1/1/2016 ; Lot 13A084 , Expires 1/1/2016 ; Lot 13B037 , Expires 2/1/2016 ; Lot 13C018 , Expires 3/1/2016 ; Lot 13D012 , Expires 4/1/2016 ; Lot 13E009’ , Expires 5/1/2016 ; Lot 13E034’ , Expires 5/1/2016 ; Lot 13F044 , Expires 6/1/2016 ; Lot 13F058 , Expires 6/1/2016 ; Lot 13G026 , Expires 7/1/2016 ; Lot 13H025 , Expires 8/1/2016 ; Lot 13H081 , Expires 8/1/2016 ; Lot 13J007 , Expires 9/1/2016 ; Lot 13M052 , Expires 11/1/2016 ; Lot 13N008 , Expires 12/1/2016 ; Lot 14A019 , Expires 1/1/2017 ; Lot 14A033 , Expires 1/1/2017 ; Lot 14B015 , Expires 2/1/2017 ; 2) Product Code: 2C1067K; Lots and Expiration Dates: Lot 11E025 , Expires 5/31/2014 ; Lot 11H035 , Expires 8/31/2014 ; Lot 11N025 , Expires 12/31/2014 ; Lot 12D061 , Expires 4/30/2015 ; Lot 12F012 , Expires 6/1/2015 ; Lot 12K024 , Expires 10/31/2015 ; Lot 13A047 , Expires…
FDA’s list runs to 2,176 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 - US Distribution to the state of FL., and to the countries of : Belgium, Denmark, Germany, Italy, Japan, Norway, Poland, South Korea, Spain, Sweden and United Arab Emirates.
The states and territories these words name
- Florida
The words say it went outside the United States too.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, 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 Apr 17, 2014.
- FDA classified it on Apr 27, 2015.
- FDA’s Enforcement Report published it on May 6, 2015.
- FDA terminated it on Jul 21, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Baxter Healthcare Corp., of Deerfield, IL.
- 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 2,176 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.