Every recall we track for Medacta Usa Inc — 12 in all — plus the complaints and injury reports the public filed about them.
Medacta recalls specific shoulder surgery tools that may cause fractures in the upper arm during procedures due to improper positioning. Affected models include sizes 7-16 with reference numbers 04.01.10.0970-0979.
Medacta recalls specific interbody fusion devices due to potential screw breakage. Affected units have UDI/DI 07630345732316 and all lot numbers. No action needed if device is not used.
Medacta recalls MectaLIF Anterior Lag Plate Flush H12 (REF 03.30.3:01) due to potential screw breakage during spinal fusion surgery. Affected units have specific UDI/DI numbers and lot numbers.
Medacta recalls MectaLIF Anterior Lag Plate Flush H18 (REF 03.30.3:04) due to potential screw breakage during spinal fusion surgery. Affected units have specific UDI/DI numbers and lot numbers.
Medact: MectaLIF Anterior Antibackout Lag Cover (REF 03.30.305) may break, causing injury. All units recalled; contact for return.
Medacta recalls MectaLIF Anterior Lag Plate Flush H14 (REF 03.30.3:02) interbody fusion devices due to potential screw breakage. All units with UDI/DI 07630345732309 are affected.
Medacta recalls MectaLIF Anterior Lag Plate Flush H10 devices with serial number 07630345732286 due to potential screw breakage during spinal fusion surgery.
Medact: NextAR Shoulder surgical tools require checking for coracoid bone stability to prevent fractures. Verify patient conditions before use to avoid bone injury during surgery.
Medacta recalls GMK Sphere CR Insert Instrument Set Size 1 due to incorrect baseplate assembly. Affected units have Lot Numbers 2109258, 2111198, or 2115530. Contact for return instructions.
Medacta recalls specific shoulder implant models (ref 04.01.0023-04.01.0055) due to potential screw insertion issues. Affected users should check their implant lot numbers.
Medacta recalls specific MiniMAX cementless hip stems due to packaging breaches reported in complaint monitoring. Affected units have unique reference and GTIN numbers listed in the recall notice.
Medacta recalls GMK knee implants with a small risk of screw back-out after surgery. Affected models include specific part numbers and serial numbers for cemented total knee replacements.
