CLASS II Device recall · Reported 26 Feb 2014 · FDA Enforcement Report

Nexgen Osteotomy Cort Bon recalled by Zimmer

Zimmer is recalling Nexgen Osteotomy Cort Bon, distributed nationwide in the US. The recall was initiated on 11 Oct 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes60114195 60595579 61077273 60187380 60610778 60796106 61137985 61249340 60105628 60595582 60919090 61277444 60330148 60732231 60945764 61283889 60219129 60579389 60756650 60965136 61207433 61242494 60244944 60579385 60756651 60965137 61233951 61593013 61887830 60105629 60166064 60224275 60244943 60337906 60461446 60586318 60595606 60696728 60808905 60906705 61018586 61103031 61180337 61249355 61341882 61422286 61526208 61636571 61717191 61770492 61887831 61929703 62048813 60213807 60331257 60579387 60941524 61233952 61687333 60099537 60139269 60194156 60244942 60330150 60436638 60614725 60681999 60838357 60945765 61089048 61207434 61378442 61585149 61770493 60105630 60191625 60200995 60610790 60858860 61180338 61770494 60139270 60209213 60310131 60579392 60713474 60906706 61089049 61378443 61902190 60503470 60678795 60897195 61233953 61770495 60124943 60230948 60420518 60676026 61056150 61445351 60177068 60330149 60504976 60671244 60897209 61146352 61770496 60294720 60503550 61018587 61585151 60233993 60501971 60834361 61160767 60105632 60503494 60586320 60595609 61238563 60125012 60504978 60844061 61265359 60266112 60503499 60860053 61207435 60209212 60382121 60491633 60671248 60847409 61070792 61238565 61497083 61911709 60099538 60395058 60503554 60682001 61228341 61266850 60160832 60367469 60503479 60858861 61207436 60310132 60491634 60671251 60991375 60105634 60139271 60213808 60330152 60461447 60652031 60861035 61180339 61422287 60135104 60194157 60266113 60334482 60436657 60503483 60667751 60834366 61146353 61445352 62143506 60125013 60213809 60330153 60503489 60965138 61504824 60177432 60263493 60503552 60858859 61331581

Quantity recalled7,044,680 total

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1020-2014
FDA event ID: 66500
Recalling firm: Zimmer, Warsaw, IN
Classification: Class II
Status: Terminated
Recall initiated: 11 Oct 2013
FDA classified: 20 Feb 2014
Reported: 26 Feb 2014
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Sterility
Device type: Other Medical Devices

Timeline

11 Oct 2013	Recall initiated by company
20 Feb 2014	Classified by FDA	+132 days
26 Feb 2014	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

NEXGEN OSTEOTOMY CORT BON. Item codes starting with 0052500

Where it was distributed

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.

Nationwide

Questions about this recall

Is Nexgen Osteotomy Cort Bon recalled?

Yes. Zimmer recalled Nexgen Osteotomy Cort Bon on 11 Oct 2013. The recall is Class II and its status is Terminated. Recall number Z-1020-2014.

Why was it recalled?

Which lots are affected?

60114195 60595579 61077273 60187380 60610778 60796106 61137985 61249340 60105628 60595582 60919090 61277444 60330148 60732231 60945764 61283889 60219129 60579389 60756650 60965136 61207433 61242494 60244944 60579385 60756651 60965137 61233951 61593013 61887830 60105629 60166064 60224275 60244943 60337906 60461446 60586318 60595606 60696728 60808905 60906705 61018586 61103031 61180337 61249355 61341882 61422286 61526208 61636571 61717191 61770492 61887831 61929703 62048813 60213807 60331257 60579387 60941524 61233952 61687333 60099537 60139269 60194156 60244942 60330150 60436638 60614725 60681999 60838357 60945765 61089048 61207434 61378442 61585149 61770493 60105630 60191625 60200995 60610790 60858860 61180338 61770494 60139270 60209213 60310131 60579392 60713474 60906706 61089049 61378443 61902190 60503470 60678795 60897195 61233953 61770495 60124943 60230948 60420518 60676026 61056150 61445351 60177068 60330149 60504976 60671244 60897209 61146352 61770496 60294720 60503550 61018587 61585151 60233993 60501971 60834361 61160767 60105632 60503494 60586320 60595609 61238563 60125012 60504978 60844061 61265359 60266112 60503499 60860053 61207435 60209212 60382121 60491633 60671248 60847409 61070792 61238565 61497083 61911709 60099538 60395058 60503554 60682001 61228341 61266850 60160832 60367469 60503479 60858861 61207436 60310132 60491634 60671251 60991375 60105634 60139271 60213808 60330152 60461447 60652031 60861035 61180339 61422287 60135104 60194157 60266113 60334482 60436657 60503483 60667751 60834366 61146353 61445352 62143506 60125013 60213809 60330153 60503489 60965138 61504824 60177432 60263493 60503552 60858859 61331581

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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