PlainRecalls
FDA Devices Moderate Class II Terminated

QuickGraft¿ Model # 430PST

Reported: October 2, 2019 Initiated: August 15, 2019 #Z-2548-2019

Product Description

QuickGraft¿ Model # 430PST

Reason for Recall

Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.

Details

Units Affected
9 Qty
Distribution
NY NC LA TX MO OH
Location
Edison, NJ

Frequently Asked Questions

What product was recalled?
QuickGraft¿ Model # 430PST. Recalled by Musculoskeletal Transplant Foundation, Inc.. Units affected: 9 Qty.
Why was this product recalled?
Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 2, 2019. Severity: Moderate. Recall number: Z-2548-2019.