FDAClass IIMarch 23, 2016

Product 20 consists of all prod oct under poduct code recall

Product 20 consists of all prod oct under poduct code: KTT and same usage: Item no: 47116201900 COMPRESSION SCREW 1/2IN 47116202300 COMPRESSION SCREW…

Why was Product 20 consists of all prod oct under poduct code 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.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

lot no.: 61678184 61839111 61852988 61862260 61875843 61882261 61898918 61974385 61988314 62002243 62002244 62024181 62031621 62090117 62109252 62263147 61875838 61895890 61895891 61912706 62037827 61649744 61660679 61764382 61882257 61887223 61988311 61988312 61988313 62009735 62037784 62090119 62109257 62153293 62160886 62263160 62109261 61396164 61634704 61664774 61777417 61777418 61782841 61782843 61782845 61782848 61810565 61810566 61810567 61810568 61810569 61810570 61810571 61839106 61839107 61839108 61839109 61852999 61853001 61853002 61853005 61875839 61875854 61882265 61887219 61887220 61893994 61894002 61915563 61915564 61915565 61938456 61938457 61938458 61938459 61980692 61980694 61980696 61980698 61985662 61985665 61985670 61985676 62009730 62009731 62009732 62009734 62017442 62017443 62017444 62024184 62024185 62024186 62031633 62038976 62038977 62038978 62090115 62097349 62097351 62097353 62120586 62120587 62120589 62120590 62120593 62134879 62134889 62134890 62150227 62150230 62150231 62153290 62153291 62153292 62160882 62160884 62193769 62193770 62193771 62204429 62204430 62204431 62204432 62204433 62263150 62263153 62263156 62263158 61649748 61782622 61782623 61782839 61810563 61810564 61839110 61852991 61852993 61875841 61875849 61882258 61887216 61887217 61898919 61985648 61985652 61985656 62002245 62002246 62002247 62009728 62009729 62024182 62024183 62031630 62090118 62118596 62134877 62150234

Product
Product 20 consists of all prod oct under poduct code: KTT and same usage: Item no: 47116201900 COMPRESSION SCREW 1/2IN 47116202300 COMPRESSION SCREW…
Recalling firm
Zimmer Manufacturing B.V.
Quantity
3415
Distribution
US Nationwide Distribution
Recall date
March 23, 2016
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls