Reported Jul 13, 2016 · Terminated
Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created…
Musculoskeletal Transplant Foundation, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Musculoskeletal Transplant Foundation, Inc. · 125 May St Ste 300 · Edison, NJ · 08837-3264
Is this the product you have?
- Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury
- It can be used in theextremities, pelvis, and spine
- Product Code227005
- Lot codes and dates
- Serial
043140468011220431404680112204314046801122043140468011220431404680112204314046801122043140468011220431404680112204314046801122043140468011220431404680112204314046801122043140468011220431404680112204314046801122043140468011220431404680112204314046801122
- Serial
- Amount recalled
- 114 units
Where it was sold
- Nationwide
Why it was recalled
AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the sterile field.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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