PET Infusion Pump
Medical device recall Z-0400-2017. Published in FDA’s Enforcement Report on Nov 23, 2016.
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 Nov 23, 2016. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 165,127 (79,714 units in U.S.) 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 Source Administration Sets (SAS) used with the Medrad Intego PET Infusion System do not meet pressure testing specifications in an occlusion situation when the product is more than one year past manufacturing date.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
PET Infusion Pump
165,127 (79,714 units in U.S.), in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Impacted Batch Numbers: 20044 8401230 20110777 20110778 20129053 20130260 20143029 20168043 20168044 20218499 20223554 20226461 20229069 50378230 50508655 50514420 50515055 50515057 50562833 50562834 50562835 50562836 50572481 50574207…
Every code shown here, 1,783 characters
Impacted Batch Numbers: 20044 8401230 20110777 20110778 20129053 20130260 20143029 20168043 20168044 20218499 20223554 20226461 20229069 50378230 50508655 50514420 50515055 50515057 50562833 50562834 50562835 50562836 50572481 50574207 50574208 50574209 50585611 50586105 50596605 50597703 50597850 50600435 50601580 50602572 50604785 50606331 50620077 50629437 50632873 50634213 50657181 50663447 50665086 50669881 50677540 50686154 50688724 50693453 50695189 50696540 50696563 50698651 50699741 50699882 50699883 50705397 50705398 50718205 50718756 50720431 50721421 50725617 50725618 50731457 50735273 50738861 50740290 50743615 50747279 50748947 50750243 50752501 50755005 50781643 50782219 50783201 50784811 50786091 50786092 50786096 50789117 50789131 50789132 50792077 50793811 50795111 50798463 50801293 50801294 50804590 50804591 50808994 50812469 50826288 50826491 50826492 50827614 50827615 50828779 50831229 50831230 50833827 50834754 50836287 50837233 50838024 50840343 50840344 50841688 50843787 50845969 50847291 50848267 50848268 50848269 50853167 50855436 50856405 50857510 50860994 50866789 50867921 50869464 50869465 50871131 50872965 50878229 50878230 50878231 50878232 50881328 50881393 50881394 50881395 50881506 50881511 50881512 50882753 50886316 50886467 50886468 50886469 50888285 50888286 50888287 50888373 50890483 50890484 50890485 50892357 50892358 50892359 50892360 60000321 60000790 60000833 60000835 60000914 60000973 60001065 60001078 60001558 60001766 60001767 60001864 60002113 60002164 60002324 60002467 60002845 60002846 60003127 60003128 60003256 60003265 60003368 60003703 60004022 60004099 60004159 60004454 60004625 60004711 60005487 60006206 60006545 60006624 60007219 60007220 60007221 60007925 60008270 60008271 60008539 60008540 60008541
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.
Distributed Nationwide and internationally to : Taiwan, Ukraine, Turkey, Thailand, Slovania, Singapore, Sweden, Saudi Arabia, Serbia, Romania, Qatar, Portugal, Poland, Panama, Oman, Norway, The Netherlands, Mexico, Malta, Morraco, Libyan, Lithuania, Lebanon, Kuwait, Italy, Israel, Hungray, United Kingdom, France, Finland, Spain, Denmark, Germany, Czech Republic, Chile, Switzerland, Belguim, Bosnia, Austria, Australia,
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?
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 Sep 30, 2016.
- FDA classified it on Nov 11, 2016.
- FDA’s Enforcement Report published it on Nov 23, 2016.
- FDA terminated it on Mar 24, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Bayer Healthcare, of Indianola, PA.
- 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.”
- 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.