Every recall we track for Stryker Leibinger GmbH & Co. KG — 23 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls ENT software version NOVA 3.6.0 RC16 for visual feedback errors during sinus surgery. Affected units may show incorrect points relative to physical reference points.
Stryker recalls 1.5/1.7MM Dynamic Mesh (56-90614) due to mislabeling as 90x90 Gold Mesh when it's actually 90x90 Blue Mesh, potentially delaying surgical procedures.
Stryker recalls unapproved TMJ reconstruction prosthesis models. This device was shipped without regulatory approval, posing potential safety risks.
Stryker recalls MEDPOR Titan OFW - MTB Right 1.0mm implants with a packaging error where the barrier layer is on the wrong side. This could affect surgical placement. Check your implant's UDI and lot number.
Stryker Leibinger recalls DirectInject cement paste system due to inability to inject paste into target location. Affected units have specific lot numbers and product codes.
Stryker recalls QUIKFLAP surgical covers (part 12-01536S) due to potential packaging compromise after 3 years. Affected units sold with serial numbers 1000232402 and 1000237513.
Stryker recalls QUIKFLAP cranium plates with part number 12-01530S due to potential packaging compromise after three years. Affected units include specific serial numbers listed in the recall notice.
Stryker Leibinger recalls QUIKFLAP cranium plates with potential packaging compromise after three years. Affected units include specific part numbers for cranial surgery. Contact for details.
Stryker recalls QUIKFLAP cranium surgical kits with potential packaging compromise after 3 years. Affected units have specific part numbers; contact Stryker for details.
Stryker recalls QuickFlap sterile procedure packs due to potential packaging compromise after 3 years, risking contamination of surgical implants.
Stryker recalls QUIKFLAP cranium plates (part 12-01531S) due to potential sterile packaging compromise after three years. Affected units sold with specific serial numbers. Contact for return instructions.
Stryker recalls AXS PP burr hole covers with potential packaging compromise after three years. Affected items include specific part numbers for cranium use. Consumers should check if their product matches the listed serials.
Stryker recalls QUIKFLAP cranium surgical covers (part 12-01528S) due to potential sterile packaging compromise after three years. Affected units sold with specific serial numbers. Consumers should contact Stryker for details.
Stryker recalls QUIKFLAP surgical covers (part 12-01534S) due to potential packaging compromise after 3 years. Affected units sold in 2021-2022; contact Stryker for details.
Stryker recalls AXS PP Burr Hole Covers due to potential sterile packaging compromise after three years. Affected items include specific part numbers for cranium surgery use.
Stryker recalls AXS PP cranium plates (part 12-01541S) due to potential sterile packaging compromise after three years. Affected units include specific serial numbers. Contact Stryker for details.
Stryker recalls 3 X 2-hole cranium plates with self-drilling screws that may have compromised sterile packaging after three years of use. Consumers should check product serial numbers to determine if affected.
Stryker recalls cranium screws with potential packaging compromise after three years. Affected units may have sterile barrier damage, risking infection. Contact for return instructions.
Stryker recalls QuickFlap sterile procedure packs that may have compromised packaging after 3 years, risking infection. Affected users should contact Stryker for details.
Stryker recalls cranium plates with potential packaging compromise after three years. Affected items have specific part numbers; stop using if packaging is damaged.
Stryker recalls QUIKFLAP surgical components due to potential sterile packaging compromise after three years. Affected items include specific part numbers for cranium use. Consumers should check product details and contact Stryker for guidance.
Stryker recalls QUIKFLAP surgical covers due to potential packaging compromise after 3 years. Affected items have specific part numbers and were sold for cranial use. Consumers should check their packaging dates and contact Stryker for details.
Stryker recalls AXS PP cranium plates with potential packaging compromise after three years. Affected units include specific part numbers; contact for return instructions.
