Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000S Axius Xpose 3 Access…
Medical device recall Z-0132-2015. Published in FDA’s Enforcement Report on Nov 5, 2014.
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 5, 2014. 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
- 16,532 units (19,270 units international) 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?
An internal finding identified the presence of pinholes/cuts in some of the Tyvek pouches of the vacuum tubing sets included as an accessory to Acrobat V Vacuum Off-Pump System, Acrobat SUV Vacuum Off-Pump System, Axius XPOSE 3 Access Device and XPOSE 4 Access Device.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Acrobat V Vacuum Off-Pump System OM-9100S Acrobat SUV Vacuum Off-Pump System OM-9000S Axius Xpose 3 Access Device XP-3000 XPOSE 4 Access Device XP-4000 Acrobat V Vacuum Off-Pump System Each Acrobat V Vacuum Off-Pump system is intended for use during performance of cardiac surgical procedures through a sternotomy incision approach.
16,532 units (19,270 units international), in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
class I 510 K exempt Acrobat V Vacuum Off-Pump System OM-9100S 25081832 25083629 25084722 25086515 25087723 25089063 25089942 25090685 25091907 25092783 25092968 25093960 25095207 25096649 25097068 25097679 25097895 25098213 Acrobat SUV…
Every code shown here, 1,693 characters
class I 510 K exempt Acrobat V Vacuum Off-Pump System OM-9100S 25081832 25083629 25084722 25086515 25087723 25089063 25089942 25090685 25091907 25092783 25092968 25093960 25095207 25096649 25097068 25097679 25097895 25098213 Acrobat SUV Vacuum Off-Pump System OM-9000S 25083904 25084006 25084498 25084648 25084928 25085094 25085850 25086057 25086330 25086468 25086786 25086869 25087249 25087330 25087412 25087793 25088394 25088704 25089154 25089224 25089724 25090578 25090748 25090943 25091171 25092128 25092272 25092690 25092813 25093167 25093281 25094024 25094065 25094473 25094712 25094860 25095107 25095600 25095769 25096128 25096305 25096404 25096913 25097097 25097336 25097417 25097747 25097801 25098540 25098968 Axius Xpose 3 Access Device XP-3000 25063171 25063264 25064005 25064805 25065216 25066072 25066261 25067242 25067493 25067915 25068869 25070671 25071619 25072468 25073684 25075060 25077055 25077999 25078510 25078808 25080773 25081495 25082997 25084179 25086061 25087498 25088896 25090502 25090832 25091779 25092248 25092884 25093619 25094030 25095768 25096118 25096687 25097508 25098402 25098904 XPOSE 4 Access Device XP-4000 25063351 25063594 25064160 25064428 25064917 25065315 25065547 25067036 25067396 25068245 25068555 25069189 25069589 25069971 25070492 25070808 25071242 25072056 25072852 25073562 25074441 25075249 25075644 25076681 25077208 25077638 25078154 25079334 25079975 25080256 25080465 25081324 25081566 25081959 25083287 25083699 25084533 25085038 25085516 25085696 25086333 25086530 25087192 25088336 25088517 25089557 25089623 25090324 25090692 25091410 25091811 25092398 25092567 25093083 25093570 25094620 25094845 25095211 25095862 25097087 25097274
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 countries of: ARGENTINA, AUSTRIA, BANGLADESH, BELARUS, BRAZIL, BRUNEI, CANADA, CHILE, CHINA, COLOMBIA, CROATIA, CZECH REPUBLIC, DENMARK, ECUADOR, GERMANY, FINLAND, FRANCE, GREECE, HONG KONG, INDICA, INDONESIA, ISRAEL, ITALY, JAPAN, MEXICO, MALAYSIA, NETHERLANDS, PANAMA, PERU, PHILIPPINES, POLAND, PORTUGAL, RUSSIA, SAUDI ARABIA, SINGAPORE, SLOVAK REPUBLIC, SOUTH KOREA, SPAIN, SWITZERLAND, TAIWAN, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM AND VIETNAM.
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 Aug 13, 2014.
- FDA classified it on Oct 24, 2014.
- FDA’s Enforcement Report published it on Nov 5, 2014.
- FDA terminated it on Mar 30, 2016.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Maquet Cardiovascular, LLC, of Wayne, NJ.
- 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
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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.