Pump 371 14F LT CMR Set
Medical device recall Z-2959-2024. Published in FDA’s Enforcement Report on Sep 11, 2024.
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 Sep 11, 2024. 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
- 43,636 units 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?
A potential device interaction between the Shockwave Coronary IVL Catheter and left-sided Impella Pumps during coronary interventions. Currently there is no Abiomed labeling (IFU etc.) content related to this potential interaction, so Abiomed will update the IFU to include information on this potential device interaction.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Pump 371 14F LT CMR Set; Product Code: 0048-0045;
43,636 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Product Code: 0048-0045; UDI-DI: 00813502011876; Serial Numbers: 381707 379142 384464 378824 378853 383418 384433 382733 384889 382279 384890 382280 384814 382281 384815 382282 382283 384816 384817 382284 384624 384625 382286 384818 384819…
Every code shown here, 1,998 characters
Product Code: 0048-0045; UDI-DI: 00813502011876; Serial Numbers: 381707 379142 384464 378824 378853 383418 384433 382733 384889 382279 384890 382280 384814 382281 384815 382282 382283 384816 384817 382284 384624 384625 382286 384818 384819 384820 384821 384822 384823 383689 382734 382735 383684 382736 382737 383686 382738 382739 383687 382740 383688 382741 383744 382742 383745 383520 383746 383521 383747 383522 383748 383749 383750 383751 383752 383753 383523 384891 383524 384892 382287 383525 383526 384893 381601 383527 381602 384894 383529 381604 384895 381605 384896 381606 381607 384897 381608 384898 381609 383798 381610 383799 383801 381325 383800 383802 381326 383803 381327 381566 381567 381568 381569 381571 381572 381573 381574 381575 383017 383291 383292 383293 383294 383295 383296 383297 383298 383299 383300 383251 383254 383256 383257 383258 383260 383261 383262 383264 383266 383267 383268 383269 383690 383691 383692 383693 383026 383241 383244 383245 383247 383248 383249 383250 382395 383252 383253 384954 384953 384952 384951 384950 384949 383019 383020 383021 383022 383023 383024 383025 384579 384580 383242 384581 383243 384582 384583 383246 384585 384586 384587 384588 384959 384899 384900 384901 384903 384904 384960 384907 384961 384962 384963 384964 384965 384966 384967 384968 384363 384364 384365 384366 384367 384368 384955 384956 384957 384958 383828 384171 383829 384172 384173 384174 384175 375965 384176 375967 375968 384177 375969 375970 384178 375971 384179 384180 384211 384212 384213 384214 384215 384217 384218 384219 384220 384231 384232 384233 384234 384235 375973 384236 384237 383945 375974 383946 383942 383948 383941 383950 380075 374496 384141 384143 384144 384145 384146 384147 384148 384149 384150 383824 383825 383827 383830 375576A 381545 375966 375972 383944 380589 380590 380592 380586 380588 380584 380585 380076 380079 380080 380081 380082 380083 380084 380320 380321 380322 380323 380324 380325 380326 380327 380329 380909 380910 380911…
FDA’s list runs to 787,544 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 Nationwide and the countries of Australia, Austria, Belgium, Brazil, Brunei Darussalam, Canada, Croatia, Czeck Republic, Denmark, Finland, France, Germany, Hong Kong, India, Ireland, Israel, Italy, Japan, Kuwait, Luxembourg, Malaysia, Mexico, Netherlands, Norway, Panama, Poland, Saudi Arabia, Serbia, Singapore, Slovenia, Spain, Sweden, Switzerland, Taiwan, U.A.E., United Kingdom.
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 5, 2024.
- FDA classified it on Sep 4, 2024.
- FDA’s Enforcement Report published it on Sep 11, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Abiomed, Inc., of Danvers, MA.
- 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 787,544 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
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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.