BioPro Recalls
37 recalls on record · August 21, 2019 to October 22, 2025 · Medical Devices
Recalls by year
19
22
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL 28 MD LT 14091 HEAD FEM
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Endo Head (Ceramic) Product ID/Description 13006 ENDO MODULAR CERAMIC SH 38 13012 ENDO MODULAR CERAMIC SH 51
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Femoral Head (Ceramic heads 28-30) Product ID/Description 19023 HEAD FEMORAL CERAMIC 28MM -3 19024 HEAD FEMO
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Bipolar Head Product ID/Description 18130 BIPOLAR HEAD 38MM 18131 BIPOLAR HEAD 39MM 18132 BIPOLAR HEAD 40MM
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Endo Head (Metal uni-polar, 38-55) Product Number/Description 10179 ENDO MD 38 10180 ENDO MD 41 10181 END
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
October 22, 2025Medical DevicesFDA
BioPro, Inc. recalls BioPro Femoral Head (Metal 22, 28, 32, 36, 40) cobalt chromium and ceramic heads Part ID/Description: 18593 HEAD FEM
Hazard: Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MS, Part ID 17198
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MS, Part ID 17197
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC M/L, Part ID 17037
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC MD, Part ID 17036
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant)TOE JOINT TITANIUM PC SM, Part ID 17035
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant)TOE JOINT TITANIUM NPC LG, Part ID 16816
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC ML, Part ID 16815
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
March 9, 2022Medical DevicesFDA
BioPro, Inc. recalls Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
Hazard: There is an incorrect statement regarding MR Compatibility in the BioPro Titanium MPJ implant IFU (IFU BP102303 rev 05) and patient implant cards (22266 rev 00) which indicates that the BioPro MPJ Implant has been tested for safety and compatibility in the MR Environment and is MR Conditional. MR Testing has not been conducted on the titanium version of the MPJ.
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls K-Wire HBS Sterile Lot, Item Number 19688 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro H
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x38, Item Number 19655 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
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
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x110, Item Number 19670 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x105, Item Number 19669 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x32, Item Number 19652 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x115, Item Number 19671 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x90, Item Number 19666 - Product Usage:Accessories to the BioPro Go-Ez screw system and the BioPro HBS Sy
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x85, Item Number 19665 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x34, Item Number 19653 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x95, Item Number 19667 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x36, Item Number 19654 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x100, Item Number 19668 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS
Hazard: Manufacturing flaw in the sterile barrier system
August 21, 2019Medical DevicesFDA
BioPro, Inc. recalls Go-EZ Screw 6.5x30, Item Number 19651 - Product Usage: Accessories to the BioPro Go-Ez screw system and the BioPro HBS S
Hazard: Manufacturing flaw in the sterile barrier system