00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622…
Medical device recall Z-1955-2016. Published in FDA’s Enforcement Report on Jun 22, 2016.
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 Jun 22, 2016. 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
- 19,884 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 Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 00720504622 ACETAB.CUPW/SH,0DEG,22MMX46MM 00720504828 ACETAB.CUPW/SH,0DEG,28MMX48MM 00720505228 ACETAB.CUPW/SH,0DEG,28MMX52MM 00720505628 ACETAB.CUPW/SH,0DEG,28MMX56MM 00720505828 ACETAB.CUPW/SH,0DEG,28MMX58MM 00720506028 ACETAB.CUPW/SH,0DEG,28MMX60MM 00720506228 ACETAB.CUPW/SH,0DEG,28MMX62MM 00720506428 ACETAB.CUPW/SH,0DEG,28MMX64MM 00721004222 ACETAB.CUPW/SH,10DEG,22MMX42MM 00721004422 ACETAB.CUPW/SH,10DEG,22MMX44MM 00721005028 ACETAB.CUPW/SH,10DEG,28MMX50MM 00721005228 ACETAB.CUPW/SH,10DEG,28MMX52MM 00721005628 ACETAB.CUPW/SH,10DEG,28MMX56MM 00721006428 ACETAB.CUPW/SH,10DEG,28MMX64MM 00721006628 ACETAB.CUPW/SH,10DEG,28MMX66MM 00721006828 ACETAB.CUPW/SH,10DEG,28MMX68MM 00721007028 ACETAB.CUPW/SH,10DEG,28MMX70MM 00725504222 ACETAB.CUP, 0 DEG, 22MM X 42MM 00725504622 ACETAB.CUP, 0 DEG, 22MM X 46MM 00725504626 ACETAB.CUP, 0 DEG, 26MM X 46MM 00725504828 ACETAB.CUP, 0 DEG, 28MM X 48MM 00725505232 ACETAB.CUP, 0 DEG, 32MM X 52MM 00725505432 ACET CUP, 0 DEG, 32MM X 54MM 00725505632 ACET CUP, 0 DEG, 32MM X 56MM 00725505828 ACETAB.CUP, 0 DEG, 28MM X 58MM 00725505832 ACET CUP, 0 DEG, 32MM X 58MM 00725506028 ACETAB.CUP, 0 DEG, 28MM X 60MM 00725506032 ACET CUP, 0 DEG, 32MM X 60MM 00725506228 ACETAB.CUP, 0 DEG, 28MM X 62MM 00725506232 ACET CUP, 0 DEG, 32MM X 62MM 00725506428 ACETAB.CUP, 0 DEG, 28MM X 64MM 00725506432 ACET CUP, 0 DEG, 32MM X 64MM 00725506628 ACETAB.CUP, 0 DEG, 28MM X 66MM 00725506632 ACET CUP, 0 DEG, 32MM X 66MM 00725506828 ACETAB.CUP, 0 DEG, 28MM X 68MM 00725506832 ACET CUP, 0 DEG, 32MM X 68MM 00725507028 ACETAB.CUP, 0 DEG, 28MM X 70MM 00725507032 ACET CUP, 0 DEG, 32MM X 70MM 00726004222 ACETAB.CUP,10 DEG, 22MM X 42MM 00726004828 ACETAB.CUP,10 DEG, 28MM X 48MM 00726005028 ACETAB.CUP,10 DEG, 28MM X 50MM 00726005228 ACETAB.CUP,10 DEG, 28MM X 52MM 00726005232 ACETAB.CUP,10 DEG, 32MM X 52MM 00726005432 ACET CUP, 10 DEG, 32MM X 54MM 00726005632 ACET CUP, 10 DEG, 32MM X 56MM 00726005832 ACET CUP, 10 DEG, 32MM X 58MM 00726006032 ACET CUP, 10 DEG, 32MM X 60MM 00726006428 ACETAB.CUP,10 DEG, 28MM X 64MM 00726006432 ACET CUP, 10 DEG, 32MM X 64MM 00726006628 ACETAB.CUP,10 DEG, 28MM X 66MM 00726006632 ACET CUP, 10 DEG, 32MM X 66MM 00726006828 ACETAB.CUP,10 DEG, 28MM X 68MM 00726006832 ACET CUP, 10 DEG, 32MM X 68MM 00726007028 ACETAB.CUP,10 DEG, 28MM X 70MM 00726007032 ACET CUP, 10 DEG, 32MM X 70MM
19,884 total, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 61868161 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 62075682 00720504622 ACETAB.CUPW/SH,0DEG,22MMX46MM 61868174 00720504828 ACETAB.CUPW/SH,0DEG,28MMX48MM 62099999 00720505228…
Every code shown here, 1,999 characters
00720504022 ACETAB.CUPW/SH,0DEG,22MMX40MM 61868161 00720504222 ACETAB.CUPW/SH,0DEG,22MMX42MM 62075682 00720504622 ACETAB.CUPW/SH,0DEG,22MMX46MM 61868174 00720504828 ACETAB.CUPW/SH,0DEG,28MMX48MM 62099999 00720505228 ACETAB.CUPW/SH,0DEG,28MMX52MM 61985379 00720505628 ACETAB.CUPW/SH,0DEG,28MMX56MM 61739647 00720505828 ACETAB.CUPW/SH,0DEG,28MMX58MM 61859335 00720506028 ACETAB.CUPW/SH,0DEG,28MMX60MM 61868180 00720506228 ACETAB.CUPW/SH,0DEG,28MMX62MM 61885454 61912432 00720506428 ACETAB.CUPW/SH,0DEG,28MMX64MM 61763307 00721004222 ACETAB.CUPW/SH,10DEG,22MMX42MM 62075683 00721004422 ACETAB.CUPW/SH,10DEG,22MMX44MM 61792574 00721005028 ACETAB.CUPW/SH,10DEG,28MMX50MM 61747148 61770547 61859658 00721005228 ACETAB.CUPW/SH,10DEG,28MMX52MM 61747106 61812211 61830726 00721005628 ACETAB.CUPW/SH,10DEG,28MMX56MM 62020209 00721006428 ACETAB.CUPW/SH,10DEG,28MMX64MM 61836505 61855146 61954911 00721006628 ACETAB.CUPW/SH,10DEG,28MMX66MM 61830949 00721006828 ACETAB.CUPW/SH,10DEG,28MMX68MM 61885408 00721007028 ACETAB.CUPW/SH,10DEG,28MMX70MM 61830844 61859307 00725504222 ACETAB.CUP, 0 DEG, 22MM X 42MM 61770545 61804351 61763316 61786342 61786341 61804383 00725504622 ACETAB.CUP, 0 DEG, 22MM X 46MM 61770407 61804495 00725504626 ACETAB.CUP, 0 DEG, 26MM X 46MM 61836909 00725504828 ACETAB.CUP, 0 DEG, 28MM X 48MM 61947556 00725505232 ACETAB.CUP, 0 DEG, 32MM X 52MM 61747107 61763580 61786278 61830727 61859504 61859551 61879091 61879090 61912430 62002120 62075898 62100011 62115299 00725505432 ACET CUP, 0 DEG, 32MM X 54MM 61763443 61786289 61812220 61854565 61868305 61879040 61912416 61947555 61985264 62013146 62066591 62115776 00725505632 ACET CUP, 0 DEG, 32MM X 56MM 61763600 61804444 61912435 62002156 62039255 62062844 62062845 62115784 00725505828 ACETAB.CUP, 0 DEG, 28MM X 58MM 61804502 61837084 00725505832 ACET CUP, 0 DEG, 32MM X 58MM 62039086 00725506028 ACETAB.CUP, 0 DEG, 28MM X 60MM 61855145 00725506032 ACET CUP, 0 DEG, 32MM X 60MM 62075897 62100842 00725506228 ACETAB.CUP, 0 DEG, 28MM X 62MM…
FDA’s list runs to 4,043 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.
Nationwide and Foreign.
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 Apr 15, 2016.
- FDA classified it on Jun 10, 2016.
- FDA’s Enforcement Report published it on Jun 22, 2016.
- FDA terminated it on Nov 29, 2017.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Zimmer Trabecular Metal Technology, Inc., of Parsippany, 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.”
- FDA’s list of codes runs to 4,043 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.