The type of knee arthroplasty a person receives depends on the extent of the damage to the joint.

The companies with the most recalls have also faced significant.

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Food and Drug Administration (FDA) issued a notice regarding the recall in March 2015, and categorized the device as a “Class 2 Recall.

According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components between 2003 and 2019.

Cardiology Infusion Therapy. Nearly 1,000 implant parts used in knee surgeries have been affected by DePuy, Zimmer-Biomet and Stryker knee replacement recalls. For Additional Information Contact.

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. class=" fc-falcon">2. Over the last decade, Smith and Nephew has recalled 15 knee replacements, including one in 2018 for 42,000 units.

Most notably, on February 22nd, Zimmer Biomet was issued a total of 5 recall orders pertaining to their Oxford product line due to potential alumina inclusion in the finished product that could lead to cracking and separation. Mar 17, 2022 · In 2010, Zimmer issued recalls for multiple knee components in its NexGen Knee Replacement system.

Aug 9, 2022 · Summaries of information about the most serious medical device recalls.

Zimmer Biomet sent an Urgent Medical Device Recall Notice dated April 2017 to all affected customers.

205-203-4058 Ext. Several prominent knee surgeons have requested a Zimmer knee implant recall of the NexGen CR-Flex due to its early failure rate.

The companies with the most recalls have also faced significant. Walter Eisner • Fri, April 10th, 2015.

Lawsuits blame manufacturers for selling defective devices.
It has had 377 separate recalls since 2003, and, again, this number reflects separate brands being recalled, not the number of individual pieces that were pulled off the market.
2 days ago · The recall impacts almost 150,000 knee replacement implants in the U.

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The firm initiated their recall to their distributors on 06/26/2017 requesting that they destroy any product. Oct 27, 2021 · The list of knee replacement recalls for 2017 below consists of only FDA recalls. org.

Jan 25, 2018 · The recall was classified as Class II, which indicates that the device is capable of causing temporary or reversible harm. According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components between 2003 and 2019. The NexGen Tibial. The Persona trabecular metal tibial plate was included in the Zimmer recall. Walter Eisner • Fri, April 10th, 2015. .

Zimmer Biomet sent an Urgent Medical Device Recall Notice dated April 2017 to all affected customers.

According to the agency's database, there were nearly 1,300 recalls on knee replacement systems or components between 2003 and 2019. .

Product Usage: The product is intended for use in knee joint replacement arthroplasties.

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12 pounds on average, while women’s knee replacements weigh.

In 2009 alone, domestic sales aone totaled more than a billion dollars.

However, this Zimmer knee replacement component was recalled by the manufacturer over reported side effects in February 2015, affecting around 12,000 individual components.