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Job Listings

Attune Tibial Loosening - Round 2

When will Depuy and JNJ actually listen?

Will marketing and management address the baseplate loosening with customers or are they afraid the lawyers will jump on the train more than they already are?

I see cases like this weekly which is why customers have switched.

DEPUY IRELAND 9616671 ATTUNE RP TIB BASE SZ 5 CEM KNEE TIBIAL TRAYBack to Search Results
Catalog Number 150610005
Device Problem Loss of or failure to bond
Event Date 06/21/2017
Event Type Injury
Event Description

The patient was revised to address limited range of motion and loosening of the tibial component at the cement to implant interface. Cement manufacturer is unknown. Update june 21, 2017: medical records received with der. After review of the medical records, the cement manufacturer is depuy. This complaint was updated on: july 18, 2017. Update 6-23-2017: medical records have been reviewed. Device experience report indicates: the patient come into surgery with very limited range of motion. Upon exposure, the surgeon indicated that the femoral component was not internally rotated. The poly and femur component were removed, the femur appeared to be well fixed. The tibia was also removed and came out with ease, the cement was attached to the bone interface not at all still attached to the tibial component. The tibia, insert and femur were revised the patella was retained. Reportability remains unchanged. Updated on 7-19-2017.

Manufacturer Narrative

If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

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The loosening of the tibia, cement to implant interface is completely out of control and the FDA or Depuy (J&J) need to address it. Hospitals and customers are getting no answers. Is there a Depuy rep or employee out there who has the stones to address the issues with Attune? What is the company telling you to say?

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When is the Attune S Plus coming out?

After lawyers get the existing pulled one from the market.

DePuy Synthes Attune Knee Implant

If you or your loved one are a current recipient of the Attune knee implant and are experiencing negative symptoms, call a New York defective medical device attorney at Rheingold, Giuffra, Ruffo & Plotkin LLP.

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Just another day at the office.

DEPUY ORTHOPAEDICS, INC. UNKNOWN ATTUNE RP TRAY SZ 6 KNEE OTHER IMPLANTBack to Search Results
Catalog Number UNK-KNEE
Device Problem Loss of or failure to bond
Event Date 07/03/2017
Event Type Injury
Event Description

The patient was revised to address pain and loosening of the tibia, cement to implant interface, depuy cement was used.

Manufacturer Narrative

Complete product detail has not been received at this time. If further information is received a follow-up medwatch will be filed as appropriate. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

Search Alerts/Recalls

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Your email address will never be used for any other reason and will never be sold to email marketers.

A reason is required.