Zimmer Hit with a Serious Hip Replacement Part Recall

Nancy Crotti, FDA recently announced a Class I designation for a Zimmer hip replacement parts recall,, Certain Zimmer M/L taper with Kinectiv technology femoral stems and necks have “unexpected amounts of manufacturing residues” that can cause serious adverse health issues, including death, according to the agency, The Zimmer femoral stems and necks are metal alloy implants used …

Class 2 Device Recall Zimmer M/L Taper Hip Prosthesis with

Class 2 Device Recall Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology: Date Initiated by Firm: May 23, 2014: Date Posted: July 10, 2014: Recall Status 1: Terminated 3 on March 06, 2015: Recall Number: Z-2035-2014: Recall Event ID: 68390: 510KNumber: K0632726 Product Classification: Prosthesis, hip, semi-constrained, metal/polymer, porous uncemented – Product Code …

Class 1 Device Recall Zimmer M/L Taper Hip Prosthesis with

Class 1 Device Recall Zimmer M/L Taper Hip Prosthesis with Kinectiv Technology: Date Initiated by Firm: May 18, 2015: Date Posted: June 08, 2015: Recall Status 1: Terminated 3 on August 02, 2016: Recall Number: Z-1699-2015 : Recall Event ID: 71272: 510KNumber: K071856 Product Classification: Prosthesis, hip, semi-constrained metal uncemented acetabular component – Product …

Zimmer Kinectiv Recall Lawsuit

ZIMMER – CLASS 1 RECALL, Although only on the market for less than one month, from March 31, 2015 through April 20, 2015, the FDA announced that a Class 1 Recall is in effect as of June 8, 2015, for Zimmer’s M/L Taper with Kinectiv® Technology,A Class 1 …

Zimmer M-L Taper Lawsuits

Zimmer M-L Taper Are Being Recalled, The U,S, Food and Drug Administration announced on June 8, 2015 that the Zimmer M/L Taper with Kinectiv Technology Prosthesis Femoral Stems and Necks hip devices are experiencing greater than expected levels of manufacturing residues, The information is based on a May 18, 2015 Zimmer-issued recall notification letter and instructions that …

Zimmer Kinectiv Hip Recall Lawsuit

A Zimmer Kinectiv hip recall lawsuit may be an option for hip replacement patients who have suffered serious complications after having hip replacement surgery, In June 2015, Zimmer, Inc, initiated a hip recall of its M/L Taper Hip Prosthesis with Kinectiv Technology hip implants, Despite claims that hip replacements help patients increase mobility and joint stability, hip replacement systems

Zimmer Initiates a Class 1 Recall of M/L Taper Hips

Zimmer Initiates Class 1 Recall of M/L Taper Hips with Kinectiv Technology, June 8, 2015 – Zimmer today announced a Class 1 Recall of a limited number of their M/L Taper Femoral Stem and Neck hip implants with Kinectiv technology, All of the affected products are being recalled and quarantined due to a manufacturing defect,

Zimmer M/L Taper Class 1 Recall

Manufacturer Zimmer introduced the M/L Taper with Kinectiv Technology on March 31, 2015, This product was on the market until April 20, 2015, On June 8, 2015, the FDA issued a class I recall for Zimmer’s M/L Taper with Kinectiv Technology, A class I recall is the most urgent of FDA recalls, indicating that “there is a reasonable probability

Zimmer Kinectiv Hip Implants

Zimmer Kinectiv Hip Recall Lawyer, Due to manufacturing negligence, and putting profit before safety, medical device recalls have been more common now than ever, But instead of placing products in pre-market trials and requiring more clinical research, medical device companies bypass consumer safety, and put thousands of patients at risk, Zimmer’s kinectiv M/L stem hip recall is just one of

Zimmer® M/L Taper Hip Prosthesis with Kinectiv® Technology

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Zimmer ® M/L Taper with Kinectiv ™ Modular Neck Technology 20% Enlarged SIZE 9 + Y 9mm aper Kinectiv Technology addresses offset restoration by offering five offsets in 4mm increments, The offset options are accomplished by offering a scope of modular necks to be used in conjunction with a +0 femoral head, which allows for a change in offset without affecting leg length, The versatility

Zimmer VerSys Hip Implant Recalled

Comparable to the VerSys system, Zimmer’s M/L Taper with Kinectiv Technology was removed from the market in April 2015, In June 2015, the FDA issued an urgent class I recall for Zimmer’s M/L Taper with Kinectiv Technology, The FDA’s recall letter announced that Zimmer found a higher than expected amount of manufacturing residue on the products, The residue can cause …

Zimmer Recalls M/L Taper Hip Stems and Necks

On June 8, 2015, Zimmer Inc, initiated a Class I Recall of its M/L Taper with Kinectiv Technology Femoral Stems and Necks, Manufacturing Residue, Due to a process monitoring failure, higher-than-expected amounts of manufacturing residues were left on the devices made fromMarch 31, 2015 through April 20, 2015, The residues can cause “serious adverse health issues including allergic reactions

Zimmer Kinective Hip Recall Lawsuits :: Chicago Medical

Zimmer is the latest manufacturer of hip replacement devices to issue a recall of its products due to the risk of severe complications and health concerns,The M/L Taper Hip Prosthesis with Kinectiv Technology was designed to be a versatile option for use in minimally invasive surgical procedures,