AFT Straight Tube recall
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic…
Why was AFT Straight Tube recalled?
3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery
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?
Lot/Serial Numbers: 03818070421114 00319018541145 00319022171149 00419019631149 09819009071105 09819036171142
- Product
- AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic…
- Recalling firm
- Musculoskeletal Transplant Foundation, Inc.
- Quantity
- 672 units
- Distribution
- US Nationwide distribution in the state of MN.
- Recall date
- May 19, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)