Reported Mar 23, 2016 · Terminated

Product 49 consists of all product under product code: JWH and same usage: Item no: 597206529 NEXGEN ALL-POLY PATELLA,…

Zimmer Manufacturing B.V.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Zimmer Manufacturing B.V. · Turpeaux Industrial Park Rd 1 km 123.4 · Mercedita, PR · 00715

Is this the product you have?

  • Product 49 consists
  • of all product under product codeJWH
  • and same usageItem
  • no597206529 NEXGEN ALL-POLY PATELLA, 597206532 NEXGEN ALL-POLY PATELLA, 597206535 NEXGEN ALL-POLY PATELLA, 597206538 NEXGEN ALL-POLY PATELLA, 597206541 NEXGEN ALL-POLY PATELLA, 598801713 NEXGEN CEMENTED STEM EXT 598801813 NEXGEN CEMENTED STEM EXT 598801913 NEXGEN CEMENTED STEM EXT 598801610 NEXGEN FLUTED STEM EXT, 1 598801611 NEXGEN FLUTED STEM EXT, 1 598801612 NEXGEN FLUTED STEM EXT, 1 598801613 NEXGEN FLUTED STEM EXT, 1 598801614 NEXGEN FLUTED STEM EXT, 1 598801615 NEXGEN FLUTED STEM EXT, 1 598801616 NEXGEN FLUTED STEM EXT, 1 598801618 NEXGEN FLUTED STEM EXT, 1 598801619 NEXGEN FLUTED STEM EXT, 1 598801620 NEXGEN FLUTED STEM EXT, 2 598801622 NEXGEN FLUTED STEM EXT, 2 598801624 NEXGEN FLUTED STEM EXT, 2 597206126 NEXGEN MICRO ALL-POLY PAT 597206129 NEXGEN MICRO ALL-POLY PAT 597206132 NEXGEN MICRO ALL-POLY PAT 597206135 NEXGEN MICRO ALL-POLY PAT for use in total knee arthroplasty
Lot codes and dates
  • lot no.:

    464 of 464 codes

    • 61901117
    • 61901118
    • 61905924
    • 61907317
    • 61919774
    • 61925086
    • 61925087
    • 61932224
    • 61932230
    • 61976473
    • 61999384
    • 61999385
    • 61999386
    • 61999389
    • 61999392
    • 61999397
    • 61999398
    • 62027343
    • 62034454
    • 62060787
    • 62074474
    • 62074475
    • 62096756
    • 62124173
    • 62124175
    • 62124176
    • 62126603
    • 62126604
    • 62132121
    • 62164944
    • 62168501
    • 62168504
    • 62168505
    • 62168506
    • 62168507
    • 62168509
    • 62168510
    • 62168511
    • 62168512
    • 62174922
    • 62174923
    • 62220941
    • 62227159
    • 62227166
    • 62249275
    • 62258601
    • 62258607
    • 62258618
    • 62258623
    • 62299435
    • 62299436
    • 62299440
    • 62318771
    • 62326940
    • 62337816
    • 62345677
    • 62345678
    • 62345679
    • 62345680
    • 62346195
Amount recalled
53338

This recall covers 72 products

The agency filed one notice per product. You are reading one of them; the other 71 are below.

59 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

As a result of the insufficient sealer calibration data for product packaged in firm's Building II between August 2010 and April 2013. The affected products are sterile.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 13, 2017 · Data as of Sep 19, 6:46 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.