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Medical device recall Z-1023-2014. 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?
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7,044,680 total, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
61547919 61954158 61241463 61821673 62188365 61564304 60919205 61666604 60928241 62086340 62296755 60611445 60841757 60863748 61187640 61224727 61261826 62062929 62173370 60550153 60588810 60828784 61018862 61110916 61159634 62296754…
Every code shown here, 1,998 characters
61547919 61954158 61241463 61821673 62188365 61564304 60919205 61666604 60928241 62086340 62296755 60611445 60841757 60863748 61187640 61224727 61261826 62062929 62173370 60550153 60588810 60828784 61018862 61110916 61159634 62296754 60576173 61209715 61564309 60575226 60595581 60623653 60749578 62316407 60611447 61255394 61364450 61382532 60611244 60817929 60863723 60563186 62268497 61547941 62137191 61892712 61901662 60668061 61584777 61059234 61403759 60497031 61303608 61875716 62087621 62138394 61906179 61919744 61853252 60945780 61403762 61868301 62123088 62330868 61552276 60973584 61159666 61209871 61491267 61731038 61906430 62154608 60806194 60940002 61092880 62304925 61598585 61698771 61712665 61902214 62148657 60612251 60658071 60980492 61072064 61160052 61261860 61642713 61722445 62296659 60715034 61018915 61036921 61136634 61179946 61377132 61504792 61564330 61598593 61652828 61662223 61746897 61885964 61902215 62062927 62166311 62166312 62167440 60664534 60611465 61121730 61491274 61542625 62170707 62296657 62304924 61138050 61392960 61509276 61591304 61662225 61751908 61875723 61885967 61902216 62113239 62183216 62308937 62322488 60715040 60715041 62134061 62292055 61407093 61509275 61564339 61598601 61751904 61928945 62183217 62292053 62330877 61575699 61403906 60699177 61591302 62127617 62301528 60545115 61504789 61698789 61863756 62109142 62296661 61261880 61403757 62123083 62296662 60595588 61407096 61633829 61788072 62296663 60593824 60841777 61424558 62268509 61509269 61580668 61631807 62330880 61234865 61286973 61521041 62049367 61241564 61542576 61751903 62147386 61478541 60588818 62118728 61403756 61598607 62044858 62329122 61547934 62147387 61478392 61575705 61788071 62329128 61712669 61005950 60945793 60595589 61765738 61036924 61668359 61478415 62330884 61110936 61675948 61138057 62301533 60717011 60611470 60656941 60863743 62330885 60715052 61287001 61751907 60600334 62296665 62327789 61651457 62292056 60862307 62077408 62180255 62296658…
FDA’s list runs to 2,240 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 2,240 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.