medical Class II Updated 2019-11-20

Orthofix Srl recalls ORTHOFIX Catalogue Number: ref: 99-91647UE, UE XCALIBER ANKL

Recalled Product

ORTHOFIX Catalogue Number: ref: 99-91647UE, UE XCALIBER ANKLE COMPLETE KIT, RX ONLY, UDI: (01)18032937169719

Hazard / Issue

As a result of complaint investigations it was determined that batches of drill bits have a geometrical detail that does not correspond to the intended design. This could result in lower cutting performance.

Issued by

FDA

Affected States: AZ, CA, FL, GA, HI, IA, IL, IN, KY, LA, MD, MI, MO, MS, NC, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV
Lot/Code Info: Lot # B1206515, B1206561, B1209206, B1211406, B1212677, B1215964, B1233839
View official government recall

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