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Merete Medical GmbH recalls OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails
Recalled November 18, 2020 · FDA recall Z-0435-2021 · Merete Medical
Hazard
Product may be mislabeled. · FDA Class II
Units
306 units
Sold at
Product was distributed in US - CA, IL, MD, OH, and NJ
Description
Product may be mislabeled.
Product
OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails
Manufacturer(s)
Merete Medical GmbH
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →