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Recalls from Penumbra, Inc.

Recalls from Penumbra, Inc. filed with the FDA, USDA FSIS, CPSC or NHTSA, 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
Sold in

1 recall that day

Penumbra System (RED 62 Reperfusion Catheter)

The Penumbra System (RED 62 Reperfusion Catheter) may fracture due to manufacturing issues.

Moderate risk, FDA, Manufacturing problem

1 recall that day

Penumbra System RED 68 Reperfusion Catheter

The Penumbra System RED 68 Reperfusion Catheter may fracture due to manufacturing issues.

Moderate risk, FDA, Manufacturing problem