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U.S. Department of Health and Human Services

Class 3 Device Recall Stryker

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 Class 3 Device Recall Strykersee related information
Date Initiated by FirmOctober 27, 2004
Date PostedFebruary 24, 2005
Recall Status1 Terminated 3 on May 31, 2005
Recall NumberZ-0556-05
Recall Event ID 30379
Product Classification Prosthesis, Knee Patellofemorotibial, Partial, Semi-Constrained, Cemented, Polymer/Metal/Polymer - Product Code NPJ
ProductThe Triathlon Posteriorly Stabilized Femoral Component.
Code Information Catalog Number--Lot Code: 5511-F-301--ER0215; 5511-F-301--PR04139; 5511-F-301--PR04664; 5511-F-301--PR04862; 5511-F-301--PR04891; 5511-F-301--PR04955; 5511-F-301--PR41122; 5511-F-301--PR4352; 5511-F-301--PR4424; 5511-F-301--PR4425; 5511-F-301--PR4427; 5511-F-301--PR4519; 5511-F-301--PR4734; 5511-F-301--PR4736;  5511-F-302--ER0184; 5511-F-302--PR04795; 5511-F-302--PR04808; 5511-F-302--PR04809; 5511-F-302--PR04810; 5511-F-302--PR04840; 5511-F-302--PR04887; 5511-F-302--PR04902; 5511-F-302--PR4113; 5511-F-302--PR41142; 5511-F-302--PR41143; 5511-F-302--PR4256; 5511-F-302--PR42561; 5511-F-302--PR4429; 5511-F-302--PR4430; 5511-F-302--PR4432; 5511-F-302--PR4520; 5511-F-302--PR4727; 5511-F-302--PR4738; 5511-F-302--PR4739; 5511-F-302--PR4774; 5511-F-302--PRO4626; 5511-F-302--PRO4627; 5511-F-302--PRO4629;  5511-F-401--PR04811; 5511-F-401--PR04848; 5511-F-401--PR04849; 5511-F-401--PR04865; 5511-F-401--PR04866; 5511-F-401--PR04867; 5511-F-401--PR04881; 5511-F-401--PR04882; 5511-F-401--PR4107; 5511-F-401--PR41073; 5511-F-401--PR4115; 5511-F-401--PR4435; 5511-F-401--PR4437; 5511-F-401--PR4718; 5511-F-401--PR4740; 5511-F-401--PR4775; 5511-F-401--PR4779;  5511-F-402--ER0219; 5511-F-402--PR04805; 5511-F-402--PR04805; 5511-F-402--PR04806; 5511-F-402--PR04850; 5511-F-402--PR04851; 5511-F-402--PR04880; 5511-F-402--PR04905; 5511-F-402--PR04906; 5511-F-402--PR4116; 5511-F-402--PR4258; 5511-F-402--PR4440; 5511-F-402--PR4442; 5511-F-402--PR4443; 5511-F-402--PR4716; 5511-F-402--PR4728; 5511-F-402--PR4777;  5511-F-501--ER0217; 5511-F-501--ER0250; 5511-F-501--PR4117; 5511-F-501--PR4118; 5511-F-501--PR4254; 5511-F-501--PR42541; 5511-F-501--PR42593; 5511-F-501--PR4418; 5511-F-501--PR4444; 5511-F-501--PR4445; 5511-F-501--PR4446; 5511-F-501--PR4448; 5511-F-501--PR4449; 5511-F-501--PR4450; 5511-F-501--PR4452; 5511-F-501--PR4524; 5511-F-501--PR4767;  5511-F-502--ER0218; 5511-F-502--PR04884; 5511-F-502--PR04885; 5511-F-502--PR05008; 5511-F-502--PR41191; 5511-F-502--PR41194; 5511-F-502--PR4379; 5511-F-502--PR4456; 5511-F-502--PR4457; 5511-F-502--PR4458; 5511-F-502--PR4459; 5511-F-502--PR4460; 5511-F-502--PR4461; 5511-F-502--PR4525; 5511-F-502--PR4526; 5511-F-502--PR4527; 5511-F-502--PR4768; 5511-F-502--PR4778;  5511-F-601--ER0185; 5511-F-601--ER0280; 5511-F-601--PR04886; 5511-F-601--PR04904; 5511-F-601--PR05021; 5511-F-601--PR05052; 5511-F-601--PR05229; 5511-F-601--PR41421; 5511-F-601--PR41422; 5511-F-601--PR41423; 5511-F-601--PR4464; 5511-F-601--PR4528; 5511-F-601--PR4529; 5511-F-601--PR4752; 5511-F-601--PR4753; 5511-F-601--PR4798; 5511-F-601--PR5026; 5511-F-601--PR5032; 5511-F-601--PR5037; 5511-F-601--PR5046; 5511-F-601--PR5108; 5511-F-601--PR5110;  5511-F-602--ER0186; 5511-F-602--ER0253; 5511-F-602--ER0254; 5511-F-602--ER0265; 5511-F-602--J66915; 5511-F-602--PR04662; 5511-F-602--PR04828; 5511-F-602--PR04863; 5511-F-602--PRO4864; 5511-F-602--PR4099; 5511-F-602--PR42731; 5511-F-602--PR4470; 5511-F-602--PR4471; 5511-F-602--PR4472; 5511-F-602--PR4754; 5511-F-602--PR4757; 5511-F-602--PR4772; 5511-F-602--PR4776; 5511-F-602--PR4781; 5511-F-602--PR4901; 5511-F-602--PR5111; 5511-F-602--PR5112.  Several units of the same lot number are reported in the quantity distributed.
Recalling Firm/
Manufacturer		 Stryker Howmedica Osteonics Corp.
325 Corporate Dr
Mahwah NJ 07430-2002
For Additional Information ContactDominick Cristofolo
201-831-5247
Manufacturer Reason
for Recall		The fatigue testing of the Triathlon PS Femoral Component does not consistently meet the requirements of the finite element analysis predicted load as delineated in the 510(k) submittal.
FDA Determined
Cause 2		Other
ActionNotification letters and Product Accountability Froms have been sent via Fedex on 10/27/2004 with return receipt.
Quantity in Commerce386 UNITS
DistributionThe product is distributed to its branches/agencies and to hospitals nationwide.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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