BioPro, Inc. recalls
Every recall we track for BioPro, Inc. — 37 in all, from 2019–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from BioPro, Inc. peaked in 2019 (21); 37 since 2017.
All FDA recall records for BioPro, Inc. 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 | 6 | 15 | 21 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 6 | 3 | 1 | 10 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 6 | 0 | 6 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for BioPro, Inc. recalls
What to do if you have a recalled BioPro, Inc. 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 BioPro, Inc. recalls
3 shown- Lower riskMedical device
BioPro, Inc. recalls BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM
BioPro recalls bipolar head implants with potential packaging defects that could compromise sterility, risking infection if implanted. Affected models include 38mm to 60mm sizes.
BioProSep 9, 2025 - Lower riskMedical device
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
BioPro recalls Titanium MPJ toe implants due to unverified MR safety claims. The implant may not be safe for MRI scans as testing was not done on the titanium version.
BioProFeb 1, 2022 - UnratedMedical device
BioPro, Inc. recalls Go-EZ Screw 6.5x120, Item Number 19672 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS
BioPro recalls Go-EZ Screw 6.5x120 (Item 19672) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioProJun 25, 2019
BioPro, Inc. recall questions
How many recalls has BioPro, Inc. had?
37 recalls from BioPro, Inc. are on record with U.S. safety agencies, from 2019–2025.
What is the most recent BioPro, Inc. recall?
BioPro, Inc. recalls BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM, dated Sep 9, 2025. Every BioPro, Inc. recall is listed on this page, newest first.
Why are BioPro, Inc. products recalled?
The most common reasons on record: Manufacturing flaw in the sterile barrier system (21).
What should I do if I have a recalled BioPro, Inc. 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 BioPro, Inc. 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.