MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID
Medical device recall Z-1035-2014. Published in FDA’s Enforcement Report on Feb 26, 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 Feb 26, 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
- 7,044,680 total 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?
Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 1 packaging operation at this facility were not properly validated. As a result, Zimmer conducted seal integrity testing to evaluate if previously packaged product from this facility met the established requirements for sterile barrier integrity. The acceptance criteria established for this testing was 99% reliability with a 90% confidence interval. These packaging tray configurations met the acceptance criteria for sterile barrier integrity of both the inner and outer trays, however, Zimmer has decided to recall all manufacturing lots that have not expired and that were sterile packaged in the ZMBV facility Building 1 packaging operations.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID
7,044,680 total, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
60169597 365445 60096116 60096117 60134409 60845244 61059560 61613250 366221 60096118 60553617 60743729 60990038 61298521 365622 60096119 60411949 60501830 60540531 60609946 60700469 61657255 365458 60110443 60154855 60187556 60301871…
Every code shown here, 1,995 characters
60169597 365445 60096116 60096117 60134409 60845244 61059560 61613250 366221 60096118 60553617 60743729 60990038 61298521 365622 60096119 60411949 60501830 60540531 60609946 60700469 61657255 365458 60110443 60154855 60187556 60301871 60484369 60590160 60716272 60768572 60887301 61118584 61211680 61304669 61589078 61619986 366386 60096121 60124827 60169413 60242838 60301886 60411970 60484390 60540735 60565849 60610009 61122126 61401537 61694181 61878452 61934378 61992515 365461 366387 367572 60109037 60110290 60124913 60169470 60204787 60242845 60326542 60395275 60423101 60474918 60484409 60768593 60845456 61199171 61298517 61613251 61817985 61992516 365499 367548 369841 60096125 60110448 60148883 60242895 60293315 60484704 60540826 60581312 60737211 61103540 61324218 61619209 61659604 61758278 61817987 366388 369882 60109039 60124924 60134410 60169479 60187599 60242901 60293321 60335415 60442118 60506747 60993378 60993379 61118585 61276626 61398796 61651794 61756168 61758280 60096126 60187653 60412010 60537009 60574597 60787916 61118586 61932403 366389 369842 60124934 60187682 60274760 60423134 60980807 61231910 61651793 61837093 365464 365604 60096127 60355236 60540889 60565935 61662668 61976171 365444 60085816 60148884 60484813 61042186 61290074 61528630 61744433 60301911 60541000 61059561 61555631 61658313 366382 60154916 60395295 60900095 61324217 60096128 60541001 61370524 365448 60096186 60553915 61496597 60096187 60096188 366307 60096189 60096190 60166763 367542 60110458 60301876 60906529 60169412 60326978 60484392 61895487 60099418 60242846 60506729 60096192 60096193 365496 60523403 60331362 365481 366300 61222214 365500 60906530 61886563 366301 60096195 60484817 61886564 365449 366304 60423158 60906531 60096202 60331367 365616 366578 367657 369317 60101998 60101999 60113196 60113197 60145797 60156493 60178358 60187897 60213589 60274027 60284125 60284126 60294382 60313728 60382721 60411695 60467652 60474624 60614956 60708479 60793758 60822078 60822089…
FDA’s list runs to 2,643 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 the countries of Belgium, Canada, Canary Islands, China, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Italy, Japan, Korea, Luxemburg, Netherlands, New Zealand, Norway, Portugal Reunion, Russian Federation, Singapore, Slovakia, Spain, Sweden, Switzerland, Turkey, Taiwan, Thailand, and 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?
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 Oct 11, 2013.
- FDA classified it on Feb 20, 2014.
- FDA’s Enforcement Report published it on Feb 26, 2014.
- FDA terminated it on Apr 14, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Zimmer, Inc., of Warsaw, IN.
- 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 2,643 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.