QuickGraft¿ recall
QuickGraft¿ Model # 430PST
Why was QuickGraft¿ 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial # 00319004921075 00319004921073 00319007681048 00319014411085 00618052231059 03319006511040 03319009191029 03319019231072 03519018121056
- Product
- QuickGraft¿ Model # 430PST
- Recalling firm
- Musculoskeletal Transplant Foundation, Inc.
- Quantity
- 9 Qty
- Distribution
- NY NC LA TX MO OH
- Recall date
- October 2, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)