XP-XP Tibial Tray - Interlok 69 mm
Medical device recall Z-2523-2019. Published in FDA’s Enforcement Report on Sep 18, 2019.
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 18, 2019. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- 44 states named in where it went
- 1282 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?
The locking bar not fully engaging
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
XP-XP Tibial Tray - Interlok 69 mm Item # 195754
1282 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
Lot Number 590860 660490 590850 560350 562180 650420 758270 841570 650430 613370 303400 589890 972740 998060 998040 972730 043990 066130 101900 174980 282760 101920 174970 207000 258020 101920R 066140 101890 101930 258030 036260 322420…
Every code shown here, 1,549 characters
Lot Number 590860 660490 590850 560350 562180 650420 758270 841570 650430 613370 303400 589890 972740 998060 998040 972730 043990 066130 101900 174980 282760 101920 174970 207000 258020 101920R 066140 101890 101930 258030 036260 322420 374530 374550 358950 358950R 036250 358940 207020 336660 207010 420360 336960 558600 558610 592310 374520 420400 592340 282770 592330 499140 499130 499130R 381700 381710 499110 322400 381720 802050 855300 802050R 802060 840700 864710 802060R 061380 223100 885070 958400 975590 975600 011450 023370 958410 984760 011440 499120 828710 166070 885060 916840 916840R 840690 558620 061390 115970 131220 115990 159300 181400 093390 181410 201940 103020 293790 223090 297190 293820 592290 418710 336120 418700 336100 418690 420380 467190 599780 511460 556570 634200 664170 705610 684910 587280 684900 297180 716090 705630 716080 715810 715790 882080 715800 715780 985910 985920 029250 906690 906710 029260 920580 072870 072890 125990 126000 162970 396350 432530 162990 221390 247330 293100 247310 247320 293110 318470 336700 318480 318500 336690 882090 389990 390020 374450 441910 478860 374420 441920 441930 478880 478890 509710 509720 543330 522630 543300 576140 576150 593600 593610 639640 639650 625500 625480 670550 450430 758520 708440 741510 570250 670560 758510 780190 833180 708470 741520 808230 808250 850930 780200 850920 873520 917620 943530 950960 873530 076670 076680 999320 183440 481860 522650 559020 570230 999440 999310 018130 999450 202940 303390 111690 219790 137500 111660 191140 512610 422510 590870
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.
State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
The states and territories these words name
44 states and territories.
Every one of them
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- District of Columbia
- Florida
- Georgia
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
- Wyoming
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 Aug 15, 2019.
- FDA classified it on Sep 12, 2019.
- FDA’s Enforcement Report published it on Sep 18, 2019.
- FDA terminated it on Apr 16, 2021.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Zimmer Biomet, 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.”
- 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.