Zimmer Biomet, Inc. recalls TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 0045000
Recalled Product
TM Ankle and Ankle Talus L/R, Item Nos. 00450001100 00450001200 00450001300 00450001400 00450001500 00450001600 00450002100 00450002200 00450002300 00450002400 00450002500 00450002600
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
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime