Every recall we track for Zimmer, Inc. — 71 in all — plus the complaints and injury reports the public filed about them.
Zimmer recalls Off-Axis Comprehensive Shoulder System model 110040242 due to plastic guides catching during reaming, potentially causing breakage. Five complaints reported.
Zimmer recalls specific Off-Axis Shoulder System guides due to plastic guides breaking during reaming, causing potential injury. Affected models include 110040240 with lot numbers 099457 and 099458.
Zimmer recalls Off-Axis Alliance Glenoid Left 4-Peg Augment Reamer Guide model 110040444 due to plastic guides catching during reaming, potentially causing breakage. Affected units sold with specific lot codes.
Zimmer recalls Off-Axis Alliance Glenoid Right 4-Peg Augment Reamer Guide model 110040476 due to plastic guides catching during reaming, causing breakage. Affected units may need repair.
Zimmer recalls Off-Axis Comprehensive Shoulder System model 110040241 due to plastic guides catching during reaming, causing breakage. Five complaints reported.
Zimmer recalls Persona Revision Femoral Distal Augment model 42-5572-066-10 due to posterior augment found in distal package. Affected patients should contact Zimmer for details.
Zimmer recalls 20-pack disposable mixing bowls with spatulas due to potential package seal failures that could compromise sterile barriers during surgery.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures. Affected implants may lead to pain, surgery, or tissue damage. Check model numbers and lot codes for recall.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected models include specific lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with potential undersized diameter that could cause fractures. Affected units may lead to pain, surgery, or tissue damage. Contact Zimmer for details.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized shaft that could fracture, causing pain, non-union, or surgery. Affected models include Lot Numbers 66717603, 66892902, and 67031550.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units have specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fracture, leading to pain, surgery, or tissue damage. Affected units include specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units include specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected models include Lot 66717602 and 66892901.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units have specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures. Affected implants may lead to pain, surgery, or tissue damage. Check model numbers 815509360 and lot numbers 66717553 or 66884563 for recall.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units have specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures. Affected implants may lead to pain, surgery, or tissue damage. Contact Zimmer for details.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units include specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures. Affected implants may lead to pain, surgery, or tissue damage. Check model numbers 815509340 and lot numbers 66717552 or 66884562.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures. Affected implants may lead to pain, surgery, or tissue damage. Check model numbers and lot codes for recall.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that could cause fractures, leading to pain, surgery, or tissue damage. Affected units have specific model and lot numbers.
Zimmer recalls Affixus Antegrade Femoral Nails with possible undersized diameter that may cause fractures. Affected implants could lead to pain, surgery, or tissue damage. Check model numbers 815509420 and lot numbers 66717556 or 66884566.
Zimmer Biomet recalls Dual Mobility Vivacit-E bearings with size mixup risk. The package labels a Size F but contains Size G implants, potentially causing improper fit.
Zimmer Biomet recalls two lots of Dual Mobility Vivacit-E bearings due to size mixup between Size F and Size G implants. This mismatch could cause improper joint fit and complications during surgery.
Zimmer Biomet recalls ceramic hip prostheses with model 802802201 due to unclear labeling on compatibility with metal and stainless steel stems. Affected users should contact Zimmer for guidance.
Zimmer Biomet recalls 22.2mm ceramic hip heads with model 802802203 due to potential incompatibility with cobalt-chrome or stainless-steel femoral stems. This may cause improper fit during hip replacement surgery.
Zimmer Biomet recalls ceramic hip prosthesis heads with incompatible labeling for cobalt-chrome or stainless-steel stems. Affected units may not fit properly, risking improper joint function.
Zimmer Biomet recalls ceramic hip prosthesis heads due to potential incompatibility with cobalt-chrome and stainless-steel femoral stems. Affected models include 22.2mm diameter, 12/14 taper, +3 neck, model 802602203.
Zimmer Biomet recalls ceramic hip prostheses with 22.2mm diameter heads that may not fit with certain stems, risking improper fit and injury. Affected units include specific model numbers and lots.
Zimmer recalls specific NexGen LPS Flex knee prostheses due to mismatched label compatibility statements. Affected units may not be safe for use with certain plates. Contact Zimmer for details.
Zimmer recalls Z1 Femoral Hip System (Product #611777612) due to potential stem inserter fracturing. Affected units include specific lot numbers and UDI-DI codes. Contact Zimmer for details.
Zimmer recalls specific NexGen LCCK Legacy Articular Surface units with incorrect metal support assembly. Affected units may have safety issues during use. Contact Zimmer for details.
Zimmer recalls specific NexGen LCCK Legacy Articular Surface models due to potential incorrect assembly of the metal support post, which could affect joint stability.
Zimmer recalls Saphena Medical Venapax XL endoscopic vessel harvesting systems due to potential endoscope slot misalignment causing surgical interference. Affected units have specific lot numbers and item codes.
Zimmer recalls hip joint implants with increased risk of postoperative femur fracture. Affected models include specific item numbers for hip arthroplasty procedures.
Zimmer recalls NexGen CR-Flex Femoral Components (Size E and E-) due to a gap in metal bonding that could cause failure. Affected items have specific UDI codes listed in the recall.
Zimmer recalls certain distal lateral fibular plates due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional fixation.
Zimmer recalls specific distal lateral fibular plates due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional procedures.
Zimmer recalls specific distal lateral fibular plates due to thread form issues that may cause improper screw mating, leading to surgery delays or loss of fixation.
Zimmer recalls specific ZPLP fibular plates due to thread form issues that may cause screws to fail, risking surgery delays or loss of fixation. Affected units include certain lot numbers and sizes.
Zimmer recalls certain ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause screws to not lock properly, risking surgery delays or loss of fixation. Affected items have specific lot numbers.
Zimmer recalls specific left fibular plates with thread issues that could lead to improper fixation during surgery. Affected units have unique lot numbers; contact Zimmer for details.
Zimmer recalls specific ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw mating, leading to surgery delays or loss of fixation. Affected items have listed lot numbers.
Zimmer recalls certain distal lateral fibular plates due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional fixation.
Zimmer recalls a specific fibular plate model due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring additional procedures. Affected units have a specific lot number and item number.
Zimmer recalls specific left fibular plates due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring additional procedures.
Zimmer recalls certain ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw fixation, risking surgery delays or loss of stability.
Zimmer recalls specific ZPLP distal lateral fibular plates due to thread form issues that may cause improper screw mating, leading to surgery delays or loss of fixation.
Zimmer recalls specific fibular plates due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring additional procedures.
Zimmer recalls specific ZPLP distal lateral fibular plates due to thread form issues that may cause improper screw mating, leading to potential delays in surgery or loss of fixation.
Zimmer recalls specific ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw fixation, risking surgery delays or additional procedures.
Zimmer recalls specific ZPLP Distal Lateral Fibular Plates due to thread form issues that may cause improper screw locking, potentially delaying surgery or requiring additional procedures.
Zimmer recalls specific distal lateral fibular plates due to thread form issues that may cause improper screw mating, potentially delaying surgery or requiring additional fixation.
Zimmer recalls specific fibular plates due to thread issues that could lead to improper screw fixation, risking surgery delays or additional procedures. Affected units have unique lot numbers and item codes.
Zimmer recalls specific left fibular plates due to thread form issues that could lead to improper screw fixation, risking surgery delays or additional procedures.
Zimmer recalls specific ZPLP Distal Lateral Fibular Plate models due to thread form issues that may cause screws to not lock properly, risking surgery delays or loss of fixation. Affected items have unique lot numbers.
Zimmer recalls specific left fibular plates for potential surgery delays due to improper screw locking. Affected items have unique lot numbers; contact Zimmer for details.
Zimmer recalls two hip implant models with incorrect size labeling. This mix-up could lead to improper fit if used, but no injuries reported. Affected units include specific item numbers and lot numbers.
