BioPro recalls

BioPro has 37 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 22 Oct 2025. 6 are still ongoing. The most frequent reason is sterility.

Total recalls37since 2019

Last 12 months0reported

Class I00% of total

Ongoing6latest 22 Oct 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 6 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 37 100%Class III 0 0%

Why biopro is recalled

Sterility2773%
Labeling Errors1027%

Product types

Hip & Knee Implants2465%
Other Medical Devices1335%

By year

2025616%
20221027%
20192157%

Ongoing biopro recalls

6 active

Reported	Class	Recall	Company	Reason	Where
22 Oct 2025Device	CLASS II	Femoral Head (Ceramic heads 28-30) Product ID/Description recalled	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Endo Head (Metal uni-polar, 38-55) Product recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Femoral Head Product ID/Description 14089 Head Femoral recalled	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Endo Head (Ceramic) Product ID/Description 13006 Endo recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Femoral Head (Metal 22, 28, 32, 36, cobalt chromium recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Bipolar Head Product ID/Description 18130 Bipolar Head recalled	BioPro	Sterility	MI, TX

All biopro recalls, newest first

37 total

Reported	Class	Recall	Company	Reason	Where
22 Oct 2025Device	CLASS II	Femoral Head (Ceramic heads 28-30) Product ID/Description recalled	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Endo Head (Metal uni-polar, 38-55) Product recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Femoral Head Product ID/Description 14089 Head Femoral recalled	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Endo Head (Ceramic) Product ID/Description 13006 Endo recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Femoral Head (Metal 22, 28, 32, 36, cobalt chromium recalled by BioPro	BioPro	Sterility	MI, TX
22 Oct 2025Device	CLASS II	Bipolar Head Product ID/Description 18130 Bipolar Head recalled	BioPro	Sterility	MI, TX
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium PC MD, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium Npc MS, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium Npc ML, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant)Toe Joint Titanium PC SM, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium PC LG, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium Npc SM, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium PC MS, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant)Toe Joint Titanium Npc LG, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium Npc MD, Part ID recalled	BioPro	Labeling Errors	Nationwide
9 Mar 2022Device	CLASS II	Titanium Mpj (Toe Implant) Toe Joint Titanium PC M/L, Part ID recalled	BioPro	Labeling Errors	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	K-Wire Single Trocar 1.1x150mm recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	K-Wire Sterile Single Trochar recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	K-Wire HBS Sterile recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	K-Wire Single Trocar 2.5x170mm recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	Go-EZ Screw recalled by BioPro	BioPro	Sterility	Nationwide
21 Aug 2019Device	CLASS II	K-Wire HBS Sterile recalled by BioPro	BioPro	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.