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Medical device recalls

Medical device recalls from FDA, newest first. Company page 2 recalls Each recall is dated by the day its recall page names (how recalls are dated).
Agency
Risk level
Status
Date
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1 recall that day

Smith & Nephew EVOS Lateral Proximal Tibia Plate

A Partial Articular Lateral Proximal Tibia Plate implant was labeled and laser etched as a Lateral Proximal Tibia Plate.

Moderate risk, FDA, Labeling error

1 recall that day

Smith & Nephew Trigen Proximal Straight Humeral Nail

The humeral nail is missing distal holes and may lead to revision surgery if implanted.

Moderate risk, FDA, Manufacturing problem