Bioventus, LLC recalls
Every recall we track for Bioventus, LLC — 2 in all, from 2019–2020 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
2 recalls since 2017.
All FDA recall records for Bioventus, LLC since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 1 | 0 | 1 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Bioventus, LLC product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Bioventus, LLC recalls
2 shown- Lower riskMedical device
Bioventus, LLC recalls EXOGEN Ultrasound Coupling Gel
Bioventus recalls EXOGEN Ultrasound Coupling Gel with potential microbial particulates. Affected units include specific part numbers and lots. Consumers should check their product details and contact Bioventus for guidance.
BioventusDec 17, 2020 - Lower riskMedical device
Bioventus, LLC recalls BIOVENTUS Bioactive Bone Graft Putty 15g Rx only/sterile. Filler device intended for use in bony voids or gaps that are
Bioventus recalls 15g sterile bone graft putty due to potential pouch puncture during shipping, which could lead to non-sterile devices and patient infections. Affected items have specific lot numbers and catalog codes.
BioventusFeb 13, 2019
Bioventus, LLC recall questions
How many recalls has Bioventus, LLC had?
2 recalls from Bioventus, LLC are on record with U.S. safety agencies, from 2019–2020.
What is the most recent Bioventus, LLC recall?
Bioventus, LLC recalls EXOGEN Ultrasound Coupling Gel, dated Dec 17, 2020. Every Bioventus, LLC recall is listed on this page, newest first.
What should I do if I have a recalled Bioventus, LLC product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Bioventus, LLC recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.