Every recall we track for Orthofix Srl — 34 in all — plus the complaints and injury reports the public filed about them.
Orthofix recalls specific Fitbone Trochanteric Nails L245mm (D9mm, Sterile) due to potential bending during insertion, requiring replacement. Affected units have lot numbers B4771336 and B4771337.
Orthofix recalls US XCaliber Ankle Complete Kit (RX only) with specific lot numbers due to drill bits that may cause lower cutting performance. Affected users should check their kit's lot number.
Orthofix recalls specific 3.2mm drill bits due to design flaws causing reduced cutting performance. Affected units have unique lot numbers and catalog codes. Consumers should check their product details to determine if they are impacted.
Orthofix recalls pelvis sterile kits with specific UDI numbers due to drill bits that may cause lower cutting performance. Affected kits require replacement.
Orthofix recalls Prefix II Diaphyseal Complete Kit (Sterile Long Screws) due to drill bits with design flaws that may cause lower cutting performance. Affected units sold outside the US.
Orthofix recalls specific elbow sterile kits due to drill bits with lower cutting performance. Affected kits have unique lot numbers and UDI codes. Consumers should check their kit details to determine if recalled.
Orthofix recalls specific batches of sterile radiolucent wrist fixator kits due to drill bits with design flaws that may cause lower cutting performance. Affected units include model ref: 99-36501 with lots B1200654 to B1232424.
Orthofix recalls specific drill bits (catalog #11007) due to lower cutting performance. Affected items have a geometrical detail mismatch. No remedy specified in official notice.
Orthofix recalls sterile ankle kits with specific lot numbers due to drill bits that may not cut properly. Affected kits were not marketed in the US.
Orthofix recalls specific lower limb diaphyseal sterile kits due to drill bits with design flaws that may cause lower cutting performance. Affected kits have unique lot numbers and require verification.
Orthofix recalls specific tibia-femur sterile kits due to drill bits with design flaws that may cause lower cutting performance. Affected kits have UDI (01)18054242S511298 and lot B1225603.
Orthofix recalls specific ankle kits with drill bits that may have lower cutting performance due to design issues. Affected units include certain lot numbers from the listed catalogue.
Orthofix recalls specific drill bits due to lower cutting performance. Affected items have unique lot numbers and are used in medical procedures. Contact Orthof: 1-800-222-4444 for details.
Orthofix recalls ankle transfix pin sterile kits with specific lot numbers due to drill bits that may cause lower cutting performance. Affected kits include lot B1200695 and B1224714.
Orthofix recalls 8mm drill bits with potential lower cutting performance due to design issues. Affected items have specific catalog numbers and lot codes. Consumers should check their product details.
Orthofix recalls specific drill bits (catalog #1100201) due to design flaw causing lower cutting performance. Affected units sold with certain lot numbers.
Orthofix recalls specific pelvis sterile kits with drill bits that may have lower cutting performance due to design issues. Affected kits include certain lots sold under catalog number 99-93501JP.
Orthofix recalls specific drill bits (catalogue ref 1100301) due to design flaw causing lower cutting performance. Affected units include certain lots and batch numbers.
Orthofix recalls specific drill bits due to design issues causing lower cutting performance. Affected items have a unique catalog number and lot numbers. Consumers should check their product details.
Orthofix recalls specific pelvis sterile kits with drill bits that may have lower cutting performance. Affected kits include lot numbers B1200694, B1204116, B1224715, B1232315. Contact Orthofix for remedy.
Orthofix recalls ankle sterile kits with specific UDI numbers due to drill bits that may cause lower cutting performance. Affected kits have UDI (01)18033509859922 and lots B1200695/B1224714.
Orthofix recalls sterile surgical kits with drill bits that may not cut properly due to design flaws. Affected kits have specific catalog numbers and lot codes. Contact Orthofix for details.
Orthofix recalls Prefix II Diaphyseal Complete Kit (Sterile No Screws) due to drill bits with lower cutting performance. Affected units sold outside US; no remedy specified.
Orthofix recalls specific drill bits (catalogue ref 13550) due to design flaw causing lower cutting performance. Affected items have specific dimensions and lot numbers.
Orthofix recalls specific drill bits (catalogue ref 1-1355001) due to lower cutting performance. Affected units have UDI codes 0118054242S10918 and lots 300244, 300243, 289816, 273348.
Orthofix recalls Galaxy Wrist Sterile Kit (catalog #99-93601) with specific lot numbers due to drill bits that may cause lower cutting performance. Affected users should check their kit's UDI and lot numbers.
Orthofix recalls specific drill bits due to a design flaw that may cause lower cutting performance. Affected items have catalogue number ref 1100101 with specific lot numbers.
Orthofix recalls specific drill bits due to design flaw that may cause lower cutting performance. Affected items have catalogue number ref 1355001 with specific lot numbers.
Orthofix recalls specific batches of XCaliber Metadiaphyseal Complete Kit (RX only) due to drill bits with design flaws that may cause lower cutting performance. Affected units have unique UDI numbers and lot codes listed in the recall.
Orthofix recalls specific batches of sterile short screws for orthopedic use due to drill bit design flaws that may cause lower cutting performance. Affected kits include model 99-92501 with lot numbers B1207286, B1207428, B1211384, B1215263.
Orthofix recalls specific drill bits due to lower cutting performance from design issues. Affected items have a catalog number and UDI. Consumers should check their product details.
Orthofix recalls specific drill bits (catalog number 1100701) due to lower cutting performance. Affected items have a geometrical detail mismatch with intended design.
Orthofix recalls specific sizes of TL-HEX TruLok Hexapod System footplates due to incompatibility with newer struts, potentially causing improper bone alignment during healing.
