Every recall we track for BioPro, Inc. — 37 in all — plus the complaints and injury reports the public filed about them.
BioPro recalls ceramic femoral head implants (28-30mm) due to potential packaging defects that could compromise sterility, risking infection after implantation.
BioPro recalls 10179-10196 Endo Head devices due to potential packaging defects that could compromise sterile barrier, risking infection if implanted.
BioPro recalls femoral head implants due to potential packaging defects that could compromise sterility, risking infection after surgery. Affected products include specific sizes and lot numbers.
BioPro recalls ceramic endoscopy heads with potential packaging defects that could compromise sterility, risking infection if implanted. Affected models include 13006-17296 series. No remedy specified.
BioPro recalls femoral head implants (22-40mm) due to potential packaging defects that could compromise sterility, risking infection after surgery. Affected units include specific part IDs and sizes.
BioPro recalls bipolar head implants with potential packaging defects that could compromise sterility, risking infection if implanted. Affected models include 38mm to 60mm sizes.
BioPro recalls certain titanium toe implants due to unverified MRI safety claims. The implants may not be safe for MRI scans as testing was not done on the titanium version.
BioPro recalls titanium toe implants due to unverified MRI safety claims. The implant may not be safe for MRI scans as testing was not done on the titanium version.
BioPro recalls Titanium MPJ toe implants due to unverified MR compatibility claims. The implant may not be safe for MRI scans as testing was not done on the titanium version.
BioPro recalls Titanium MPJ toe implants (Part ID 17035) due to unverified MR compatibility claims. Patients may face risks during MRI scans if the implant is not properly tested for safety in magnetic fields.
BioPro recalls Titanium MPJ toe implants due to unverified MR compatibility claims. The titanium version has not been tested for MRI safety, risking patient harm during scans.
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.
BioPro recalls Titanium MPJ toe implants due to unverified MRI safety claims. The titanium version hasn't been tested for MR compatibility, risking unsafe scans.
BioPro recalls Titanium MPJ toe implants due to unverified MRI safety claims. The implant may not be safe for MRI scans as testing was not done on the titanium version.
BioPro recalls Titanium MPJ toe implants (Part ID 16814) due to unverified MR safety claims. Patients may face risks during MRI scans if the implant is not properly tested for compatibility.
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.
BioPro recalls Go-EZ Screw 6.5x85 (Item 19665) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories for the BioPro HBS system.
BioPro recalls Go-EZ Screw 6.5x110 (Item 19670) due to a manufacturing flaw in the sterile barrier system. This could affect orthopedic surgical procedures.
BioPro recalls K-Wire Single Trocar 1.1x150mm (Item OL15011S) due to a manufacturing flaw in the sterile barrier system. This may affect orthopedic surgical procedures.
BioPro recalls Go-EZ Screw 6.5x90 (Item 19666) due to a manufacturing flaw in the sterile barrier system. This may affect orthopedic surgical procedures.
BioPro recalls Go-EZ Screw 6.5x115 (Item 19671) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls K-Wire Sterile Single Trochar (Item 19106) due to a manufacturing flaw in the sterile barrier system. This could affect orthopedic surgical procedures. Learn if your item is recalled and what to do.
BioPro recalls sterile K-Wire HBS Lot 19688 due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories for the BioPro Go-Ez screw system.
BioPro recalls Go-EZ Screw 6.5x105 (Item 19669) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls Go-EZ Screw 6.5x32 (Item 19652) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls Go-EZ Screw 6.5x36 (Item 19654) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls K-Wire Single Trocar 2.5x170mm (Item OL17025S) due to a sterile barrier manufacturing flaw. This device is used in orthopedic surgery but not for spine procedures. Affected units were made between April 2019 and Lot 123218.
BioPro recalls Go-EZ Screw 6.5x100 (Item 19668) due to a manufacturing flaw in the sterile barrier system. This could affect surgical safety during orthopedic procedures.
BioPro recalls Go-EZ Screw 6.5x30 (Item 19651) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls K-Wire HBS Sterile accessories (Item 19688) due to a manufacturing flaw in the sterile barrier system. These accessories are for orthopedic surgery but not spine procedures. Affected units have UDI M209196880 and lot 122572 from April 2019.
BioPro recalls K-Wire Sterile Single Trochar .045 (Item 19108) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with BioPro Go-Ez screw systems.
BioPro recalls K-Wire Single Trocar 1.6x150mm (Item OL15016S) due to a manufacturing flaw in the sterile barrier system. This could affect orthopedic surgery accessories.
BioPro recalls Go-EZ Screw 6.5x38 (Item 19655) due to a sterile barrier manufacturing flaw that could compromise surgical safety. Affected units include those with UDI M209196550 and lot 123109 from April 2019.
BioPro recalls Go-EZ Screw 6.5x95 (Item 19667) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls Go-EZ Screw 6.5x34 (Item 19653) due to a manufacturing flaw in the sterile barrier system. This affects orthopedic surgical accessories used with the BioPro HBS system.
BioPro recalls K-Wire Single Trocar 2.5x150mm (Item OL15025S) due to a manufacturing flaw in the sterile barrier system. This accessory is used in orthopedic surgery but not for spine procedures. Affected units were manufactured from April 24, 2019.
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.
