FDA recall record

Zimmer Manufacturing B.V NexGEN System REF 5980-37-01 Tibial Component Size Stemmed 3 recall — FDA Z-0590-2016

A product complaint was received stating that a carton labeled as a Precoat Stemmed Tibia Size 3 was opened for use and the contents were a non-augmented…

Class IIclassification
Z-0590-2016official record ID
Jan 13, 2016report date

Recall record at a glance

Official recordZ-0590-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmZimmer Manufacturing B.V.
Report dateJan 13, 2016
Recall initiation dateDec 3, 2015
Quantity384 distribution events; 1 unit was returned leaving 383 units .
LocationMercedita, PR, United States

Official product description

NexGEN System REF 5980-37-01 Tibial Component Size Stemmed 3 Precoat, and REF 5986-37-01 Nonaugmentable Tibial Component Option CR/PS/LPS Size Stemmed 3. Tibial component of implanted knee prosthesis.

Why the product was recalled

A product complaint was received stating that a carton labeled as a Precoat Stemmed Tibia Size 3 was opened for use and the contents were a non-augmented Stemmed Tibia Plate size 3.

Distribution information

Worldwide Distribution to Germany, Belgium, Denmark, France, UK, Greece, Ireland, Netherlands, Norway, Russian Fed., Saudi Arabia, Sweden, and Thailand.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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