medical Class II Updated 2019-11-13

Zimmer Biomet, Inc. recalls Periarticular locking plate elbow-sterile, Item Nos. 472358

Recalled Product

Periarticular locking plate elbow-sterile, Item Nos. 47235800503 47235800509 47235800511 47235800515 47235800519 47235800603 47235800605 47235800607 47235800609 47235800611 47235800615 47235800619 47235800705 47235800711 47235800715 47235800803 47235800805 47235800807 47235800811 47235800815 47235800911 47235800913 47235800915 47235801209 47235801211 47235801213 47235801215 47235802305 47235802307 47235802311 47235802315 47235802405 47235802407 47235802409 47235802411 47235802415 47235810707 47235810711 47235810715 47235810805 47235810807 47235810811 47235810815


Hazard / Issue

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All product manufactured prior to January 2014.
View official government recall

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