Hip Components: INSERT MOBILE “COLLEGIA” TAILLE 58*28, OT22C58
Medical device recall Z-0183-2013. Published in FDA’s Enforcement Report on Nov 7, 2012.
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 7, 2012. 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
- 31,566 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?
There may be inaccuracies on the labeled shelf life on all products packaged at the Toulon, France facility.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Hip Components: INSERT MOBILE “COLLEGIA” TAILLE 58*28, OT22C58, Lot Numbers: W07335080 and X06391225 INSERT MOBILE “COLLEGIA” TAILLE 60*28, OT22C60, Lot Number: X06391226 TETE INOX “COLLEGIA” T 28/0 CONE 6 DEG. -N30NW-, OT32H28, Lot Numbers: 068573172 and X03396534 PROFEMUR(R) Z FEMORAL STEM S 1 CEMENT LESS, PHA00232, Lot Number: X05420041 PROFEMUR(R) Z FEMORAL STEM S 5 CEMENT LESS, PHA00240, Lot Number: V03156757 PROFEMUR(R) Z FEMORAL STEM S 8 CEMENT LESS, PHA00246, Lot Number: X05410982 PROFEMUR(R) Z FEMORAL STEM S 9 CEMENT LESS, PHA00248, Lot Numbers: V01132375, W03314591, X01383213, X02388533, X03396459, X04401274, and X07428776 REVISION SHELL “PROCOTYL(R) E” SIZE 52/60 G1 T/P COATED, PHA00370, Lot Number: X10410887 REVISION SHELL “PROCOTYL(R) E” SIZE 54/62 G1 T/P COATED, PHA00372, Lot Number: X05391267 REVISION SHELL “PROCOTYL(R) E” SIZE 56/64 G1 T/P COATED, PHA00374, Lot Number: X10418370 REVISION SHELL “PROCOTYL(R) E” SIZE 60/68 G2 T/P COATED, PHA00378, Lot Number: X10410890 REVISION SHELL “PROCOTYL(R) E” SIZE 62/70 G2 T/P COATED, PHA00380, Lot Number: X04391099 REVISION SHELL “PROCOTYL(R) E” SIZE 64/72 G2 T/P COATED, PHA00382, Lot Numbers: V07227366, X01372961, X02383420, and X10410892 REVISION SHELL “PROCOTYL(R) E” SIZE 66/74 G3 T/P COATED, PHA00384, Lot Numbers: X05391100 and X05391265 REVISION SHELL “PROCOTYL(R) E” SIZE 68/76 G3 T/P COATED, PHA00386, Lot Number: X01372963 STEM REVISION “PROFEMUR(R) Z” SIZE 3, PHA00606, Lot Numbers: X01399395, X03393766, and X04393775 STEM REVISION “PROFEMUR(R) Z” SIZE 4, PHA00608, Lot Numbers: X02399397, X03393767, and X04393776 STEM REVISION “PROFEMUR(R) Z” SIZE 5, PHA00610, Lot Numbers: X03393768, X03399398, X03400451, X04393777, and X04400452 STEM REVISION “PROFEMUR(R) Z” SIZE 6, PHA00612, Lot Numbers: W12238302, X03393769, X03399400, X03400453, X04393778, and X04400454 STEM REVISION “PROFEMUR(R) Z” SIZE 7, PHA00614, Lot Numbers: X01238303, X03393770, X03399401, X03400455, X04393779, and X04400456 STEM REVISION “PROFEMUR(R) Z” SIZE 8, PHA00616, Lot Numbers: X01238304, X01399402, X03393771, X03400458, X04393780, and X04400459 STEM REVISION “PROFEMUR(R) Z” SIZE 9, PHA00618, Lot Numbers: X01238305, X03393772, X03399404, and X04393781 STEM REVISION “PROFEMUR(R) Z” SIZE 10, PHA00620, Lot Numbers: X02399405, X03393773, and X04393782 STEM REVISION “PROFEMUR(R) Z” SIZE 11, PHA00622, Lot Numbers: X02377571, X03393774, and X04393783 CROCHET POUR COTYLE “PROCOTYL(R) E” L=18 (VERSION 3, PHA01106, Lot Numbers: V0181677, X03391269, and X03396706 CROCHET POUR COTYLE “PROCOTYL(R) E” L=23 (VERSION 3, PHA01107, Lot Numbers: U0366131, V0271861, W11376812, and X03391270 ILIAC PLATE “L” SHAPE “PROCOTYL(R) E” LEFT, PHA01110, Lot Number: X05420073 ILIAC PLATE “T” SHAPE “PROCOTYL(R) E” LEFT, PHA01120, Lot Number: X03396709 ILIAC PLATE “T” SHAPE “PROCOTYL(R) E” RIGHT, PHA01122, Lot Numbers: W07327875, X03391271, and X06401587 ILIAC PLATE DOUBLE “PROCOTYL(R) E” LEFT 4 HOLES, PHA01134, Lot Number: X03396707 ILIAC PLATE DOUBLE “PROCOTYL(R) E” RIGHT 4 HOLES, PHA01144, Lot Number: X03396708 ILIAC PLATE DOUBLE “PROCOTYL(R) E” RIGHT 5 HOLES, PHA01145, Lot Number: X03396359 PROFEMUR(R) NECK NEUTRALSHORT SHORT, PHA01202, Lot Numbers: U0781477, V02143965, V05185849, and X06420151 PROFEMUR(R) NECK NEUTRAL LONG, PHA01204, Lot Numbers: U0671647 and X03396401 PROFEMUR(R) NECK A/R VAR/VAL 2 SHORT, PHA01212, Lot Numbers: U0681198, U1185239, W12383174, X01388472, X02396405, X04401230, and X05418352 PROFEMUR(R) NECK A/R VAR/VAL 2 LONG, PHA01214, Lot Numbers: W07334963, W09359069, X02388473, X02396406, X05401242, and X05418353 PROFEMUR(R) NECK A/R VAR/VAL 1 SHORT, PHA01222, Lot Numbers: W09359061, X03396407, X04401231, X10420159, and X10428842 PROFEMUR(R) NECK A/R VAR/VAL 1 LONG, PHA01224, Lot Numbers: U1185241, V06215432, X01388475, X02396408, X04401232, X05418355, and X10420160 PROFEMUR(R) NECK 8DG A/R SHORT, PHA01232, Lot Numbers: V0821
31,566 units, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
INSERT MOBILE “COLLEGIA” TAILLE 58*28, OT22C58, Lot Numbers: W07335080 and X06391225 INSERT MOBILE “COLLEGIA” TAILLE 60*28, OT22C60, Lot Number: X06391226 TETE INOX “COLLEGIA” T 28/0 CONE 6 DEG. -N30NW-, OT32H28, Lot Numbers: 068573172 and…
Every code shown here, 1,998 characters
INSERT MOBILE “COLLEGIA” TAILLE 58*28, OT22C58, Lot Numbers: W07335080 and X06391225 INSERT MOBILE “COLLEGIA” TAILLE 60*28, OT22C60, Lot Number: X06391226 TETE INOX “COLLEGIA” T 28/0 CONE 6 DEG. -N30NW-, OT32H28, Lot Numbers: 068573172 and X03396534 PROFEMUR(R) Z FEMORAL STEM S 1 CEMENT LESS, PHA00232, Lot Number: X05420041 PROFEMUR(R) Z FEMORAL STEM S 5 CEMENT LESS, PHA00240, Lot Number: V03156757 PROFEMUR(R) Z FEMORAL STEM S 8 CEMENT LESS, PHA00246, Lot Number: X05410982 PROFEMUR(R) Z FEMORAL STEM S 9 CEMENT LESS, PHA00248, Lot Numbers: V01132375, W03314591, X01383213, X02388533, X03396459, X04401274, and X07428776 REVISION SHELL “PROCOTYL(R) E” SIZE 52/60 G1 T/P COATED, PHA00370, Lot Number: X10410887 REVISION SHELL “PROCOTYL(R) E” SIZE 54/62 G1 T/P COATED, PHA00372, Lot Number: X05391267 REVISION SHELL “PROCOTYL(R) E” SIZE 56/64 G1 T/P COATED, PHA00374, Lot Number: X10418370 REVISION SHELL “PROCOTYL(R) E” SIZE 60/68 G2 T/P COATED, PHA00378, Lot Number: X10410890 REVISION SHELL “PROCOTYL(R) E” SIZE 62/70 G2 T/P COATED, PHA00380, Lot Number: X04391099 REVISION SHELL “PROCOTYL(R) E” SIZE 64/72 G2 T/P COATED, PHA00382, Lot Numbers: V07227366, X01372961, X02383420, and X10410892 REVISION SHELL “PROCOTYL(R) E” SIZE 66/74 G3 T/P COATED, PHA00384, Lot Numbers: X05391100 and X05391265 REVISION SHELL “PROCOTYL(R) E” SIZE 68/76 G3 T/P COATED, PHA00386, Lot Number: X01372963 STEM REVISION “PROFEMUR(R) Z” SIZE 3, PHA00606, Lot Numbers: X01399395, X03393766, and X04393775 STEM REVISION “PROFEMUR(R) Z” SIZE 4, PHA00608, Lot Numbers: X02399397, X03393767, and X04393776 STEM REVISION “PROFEMUR(R) Z” SIZE 5, PHA00610, Lot Numbers: X03393768, X03399398, X03400451, X04393777, and X04400452 STEM REVISION “PROFEMUR(R) Z” SIZE 6, PHA00612, Lot Numbers: W12238302, X03393769, X03399400, X03400453, X04393778, and X04400454 STEM REVISION “PROFEMUR(R) Z” SIZE 7, PHA00614, Lot Numbers: X01238303, X03393770, X03399401, X03400455, X04393779, and X04400456 STEM REVISION “PROFEMUR(R) Z” SIZE…
FDA’s list runs to 44,081 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 Internationally to Canada, Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Greece, Italy, Latvia, Lithuania, Norway, Poland, Portugal, Serbia, Slovakia, Slovenia, Spain, The Netherlands, Argentina, Brazil, Chile, China, Japan, Taiwan, Turkey, United Arab Emirates, Australia, South Africa, Russia, 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 Sep 5, 2012.
- FDA classified it on Oct 31, 2012.
- FDA’s Enforcement Report published it on Nov 7, 2012.
- FDA terminated it on Jan 7, 2014.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Wright Medical Technology Inc, of Arlington, TN.
- 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 44,081 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.