Every recall we track for Linkbio Corp. — 50 in all — plus the complaints and injury reports the public filed about them.
LinkBio recalls its CORE Workstation component due to potential incorrect "Planning Date" display on the Start Case menu. Affected units have product code 87-9136 and all serial numbers.
Linkbio recalls SymphoKnee System L-Shaped Femoral Augment (Sz 5-6 Tilastan) due to incorrect implant packaging. This could lead to wrong implant installation during knee replacement surgery.
Linkbio recalls all LINK SLED Knee System poly tibial components (13mm x 50mm) with item number 15-2028/08 due to potential early loosening from improper surgical technique. Affected patients should contact Linkbio for guidance.
Linkbio recalls all LINK SLED Knee System poly tibial components (13mm x 45mm) due to potential early joint failure from improper implant positioning during surgery.
Linkbio recalls all LINK SLED Knee System poly tibial components (7mm x 55mm) due to potential early loosening from improper surgical placement. Affected patients should consult their surgeon for evaluation.
Linkbio recalls medium-sized ENDOSLED knee implants due to potential early loosening from improper surgical technique. Affected items have specific item numbers and expiration dates.
Linkbio recalls LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, LARGE (Item 15-2220/60) due to potential early implant failure from improper surgical technique.
Linkbio recalls all LINK SLED Knee System poly tibial components (9x58mm) due to potential early loosening from improper surgical technique. Affected items have specific item numbers and expiration dates.
Linkbio recalls specific knee implant models due to risk of early loosening or wear from improper surgical technique, potentially requiring revision surgery.
Linkbio recalls ENDO MODEL SLED TIBIAL COMP 9 MM X 45 MM knee implants due to potential early failure from improper surgical installation. Affected units have specific item numbers and expiration dates.
Linkbio recalls all LINK SLED Knee System poly tibial components (13mm x 55mm, item 15-2028/12) due to potential early loosening from improper surgical technique. Affected patients should consult their surgeon.
Linkbio recalls specific knee implants due to risk of early loosening from improper installation. Affected units have item number 15-2230/07. Owners should contact for details.
Linkbio recalls all LINK SLED Knee Systems with 9mm x 45mm poly tibial components (item 15-2028/02) due to potential early joint failure from improper implant positioning during surgery.
Linkbio recalls Endo Model SLED TIBIAL COMP 11mm x 45mm knee implants due to risk of early loosening from improper placement. All units with item number 15-2030/03 are affected.
Linkbio recalls POREX ENDO MODEL SLED TIBIAL COMP 11 MM X 45 MM knee implants due to potential early loosening from improper surgical technique. Affected units have specific item numbers and expiration dates.
Linkbio recalls specific knee implants due to risk of early loosening from improper installation, requiring potential revision surgery. Affected units include POREX ENDO MODEL SLED TIBIAL COMP 13mm x 55mm with item number 15-2230/12.
Linkbio recalls its ENDO MODEL SLED TIBIAL COMP 8mm x 55mm knee implant due to potential early loosening from improper placement. Affected units have specific item numbers and expiration dates. Contact Linkbio for details.
Linkbio recalls ENDO model knee implants due to potential early loosening from improper placement or cementing, risking revision surgery.
Linkbio recalls LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 55 MM (Item 15-2230/10) due to potential early loosening from improper implant positioning or cementing. Affected patients should contact Linkbio for guidance.
Linkbio recalls its ENDO model SLED TIBIAL COMP 13mm x 50mm knee implant due to potential early revision surgery from improper implant positioning or cementing. Affected patients should contact Linkbio for guidance.
Linkbio recalls its ENDO model SLED Knee System (item 15-2030/10) due to potential early loosening from improper implant positioning. Affected users should contact Linkbio for guidance.
Linkbio recalls ENDO model knee implants due to early loosening from improper installation. Affected units have specific item numbers and expiration dates.
Linkbio recalls its ENDO model knee implant due to potential early loosening from improper surgical technique, requiring revision surgery. Affected units have specific item numbers and expiration dates.
Linkbio recalls all LINK SLED Knee System poly tibial components (7mm x 45mm) due to potential early loosening from improper surgical installation. Affected units may require revision surgery sooner than expected.
Linkbio recalls LINK SLED Knee System (item 15-2020/40) due to potential early implant loosening from improper surgical technique. Affected patients should consult their surgeon for possible revision.
Linkbio recalls all LINK SLED Knee System poly tibial components (11x58mm) due to potential early loosening from improper surgical installation. Affected patients should consult their surgeon for possible revision.
Linkbio recalls specific knee implant models due to risk of early loosening or wear from improper surgical technique, potentially requiring revision surgery.
Linkbio recalls all LINK SLED Knee System poly tibial components (9mm x 55mm) due to potential early loosening from improper surgical placement. Affected patients should contact Linkbio for guidance.
Linkbio recalls its ENDO model SLED TIBIAL COMP knee implant due to potential early loosening from improper placement. Affected units have specific item numbers and expiration dates. Contact Linkbio for details.
Linkbio recalls ENDO model SLED TIBIAL COMP knee implants due to potential early revision surgery from improper implant positioning or cementing technique.
Linkbio recalls POREX ENDO MODEL SLED TIBIAL COMP 8mm x 45mm knee implants due to early loosening risks from improper installation. Affected units have specific item numbers and expiration dates.
Linkbio recalls specific knee implants due to potential early revision surgery from improper implant positioning or cementing. Affected models include ENDO MODEL SLED TIBIAL COMP 11 MM X 55 MM with item number 15-2030/11. No immediate action needed but consult your surgeon.
Linkbio recalls all LINK SLED Knee System poly tibial components (9mm x 50mm) due to potential early loosening from improper surgical placement. Affected items have specific item numbers and expiration dates.
Linkbio recalls all LINK SLED Knee System poly tibial components (7mm x 50mm) due to potential early joint failure from improper implant positioning during surgery. Affected units have specific item numbers and expiration dates.
Linkbio recalls specific knee implants due to potential early loosening or wear from improper surgical technique, requiring revision surgery. Affected models include POREX ENDO MODEL SLED TIBIAL COMP 13mm x 50mm with item number 15-2230/08.
Linkbio recalls LINK SLED Knee System (item 15-2020/60) due to potential early implant failure from improper surgical technique. Affected patients should contact Linkbio for guidance.
Linkbio recalls all LINK SLED Knee Systems with specific poly tibial components (11mm x 45mm) due to potential early loosening from improper implant positioning during surgery, requiring possible revision surgery.
Linkbio recalls specific knee implants due to potential early loosening from improper placement or cementing, requiring surgical revision. Affected units have item number 15-2230/02 and UDI-DI 04026575429127.
Linkbio recalls specific knee implants due to potential early loosening from improper installation. Affected models include POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 50 MM with item number 15-2230/06. Owners should contact Linkbio for details.
Linkbio recalls all LINK SLED Knee System poly tibial components (13x58mm) due to potential early loosening from improper surgical placement. Affected patients should consult their surgeon for possible revision.
Linkbio recalls its ENDO model SLED Knee System (13mm x 45mm) due to potential early implant loosening from improper surgical technique. Affected units include all lot numbers with item number 15-2030/04.
Linkbio recalls LINK SLED Knee System (item 15-2020/46) due to potential early implant failure from improper surgical technique. Affected users should contact Linkbio for details.
Linkbio recalls its LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP, SMALL (Item 15-222:40) due to potential early implant loosening from improper positioning or cementing. Affected users should contact Linkbio for details.
Linkbio recalls medium-sized POREX ENDO SLED KNEE FEM COMP implants for potential early loosening from improper surgical placement. Affected units sold with item number 15-222:52.
Linkbio recalls all LINK SLED Knee System poly tibial components (11mm x 55mm) due to early aseptic loosening from improper implant positioning or cementing technique, potentially requiring revision surgery.
Linkbio recalls specific knee implants for potential early loosening from improper installation. Affected units have item number 15-2230/15. Owners should contact Linkbio for details.
Linkbio recalls medium/small LINK SLED Knee System POREX ENDO SLED KNEE FEM COMP (item 15-2220/46) due to potential early loosening from improper implant placement. Affected patients should consult their surgeon.
Linkbio recalls all LINK SLED Knee System poly tibial components (11mm x 50mm) due to potential early loosening from improper implant positioning or cementing technique.
Linkbio recalls specific knee implants due to potential early loosening or wear from improper installation, risking revision surgery. Affected models include POREX ENDO MODEL SLED TIBIAL COMP 11mm x 55mm with item number 15-2230/11.
Linkbio recalls all LINK SLED Knee System poly tibial components (7mm x 58mm) due to potential early loosening from improper surgical placement. Affected patients should consult their surgeon for possible revision.
