Every recall we track for Stryker GmbH — 75 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 60mm (Catalog 50796060) due to potential cracking after cleaning and sterilization. Affected items may need replacement.
Stryker recalls specific connecting rod micros due to potential cracking after cleaning and sterilization. Affected items have catalog number 50796050 and GTIN 04546540389916. No remedy is stated in the recall notice.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 150mm (Catalog 50796150) due to potential cracking after cleaning and sterilization. Affected units may require replacement.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 120mm (Catalog 50796120) due to potential cracking after cleaning and sterilization. All units are affected.
Stryker recalls specific connecting rod micros due to potential cracking after cleaning and sterilization. Affected items have catalog number 50796030 and GTIN 04546540389893. No remedy is listed in the recall notice.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 90mm (Catalog 50796090) due to potential cracking after cleaning and sterilization. All units are affected.
Stryker recalls Hoffmann II Connecting Rod Micro 3 x 40mm (Catalog 50796040) due to potential cracking after cleaning and sterilization. Affected units may require replacement.
Stryker recalls Gamma4 Right Long Nail (catalog 84250320S) due to being manufactured with left nail geometry. This could cause improper function in surgical procedures.
Stryker recalls specific femoral nails that were labeled incorrectly as left but contained right nails, or vice versa. This could lead to improper surgical use. Affected items have catalog number 1851-0830S and batch lot K09F17F.
Stryker recalls LEFT T2 GTN 8x300 mm nails that were mislabeled as left but contained right nails and vice versa. This mix-up could lead to incorrect surgical use.
Stryker recalls Guide Wire with Ruler Tube 3x1000 mm DIA (Catalog 2351-3100S) due to risk of metal ring detaching during surgery. Affected units include specific lot numbers from 2016-2018.
Stryker recalls Guide Wire with Ruler Tube 3x800 mm DIA (catalog 2351-3080S) due to risk of metal ring detaching during surgery. Affected units have specific lot numbers.
Stryker recalls Hoffman LRF Wire Tensioner REF 4933-9-100 due to potential wire tension misalignment from a loose adjustment ring. Affected units include Lot #J43995 with UDI-DI 07613252611035.
Stryker recalls specific models of Hoffmann LRF Bone Transport Struts due to oversized thread pitch causing improper locking. Affected units have serial numbers listed in the recall notice.
Stryker recalls Smart Toe II Intramedullary Arthrodesis Implants with potential nickel sensitivity label errors. Affected models have a label showing 'Indicated for patients with Nickel sensitivity' instead of 'Not Indicated'.
Stryker recalls elastic T2 Tibia SPI sleeves with incorrect size labeling. The inner diameter differs from the box label, potentially causing improper nail insertion. Affected units include specific catalog numbers and lot numbers.
Stryker recalls elastic T2 Tibia SPI sleeves with incorrect inner diameter labeling. This may cause improper nail insertion. Affected units have specific catalog and lot numbers.
Stryker recalls Osteosynthesis Compression Staple EasyClip products for potential nickel release in children under 20 kg when 2+ implants are used. Affected models include EasyClip and EasyClip Xpress sizes up to 25x22x22mm.
Stryker recalls specific locking screws due to potential blister pack contamination. Affected items have catalog number 18965045S and lot numbers K02C1BB through K031B70. Contact Stryker for details.
Stryker recalls specific end cap implants due to potential blister pack compromise affecting sterility. This could lead to infection if used improperly.
Stryker recalls locking screws with catalog number 17965035S due to potential blister pack compromise affecting sterility. This risks infection during surgical use.
Stryker recalls specific locking screws due to potential blister pack compromise affecting sterility. Affected items have catalog number 18965035S and lot numbers listed. Consumers should contact Stryker for details.
Stryker recalls specific locking screws due to potential blister pack compromise affecting sterility. Patients using these implants may face infection risks if the packaging is not properly sealed.
Stryker recalls specific locking screws due to blister pack seal risks. This could compromise sterility during surgery. Affected units have catalog number 18965030S and lot numbers K0207B0, K02C1A8, K02C1A9, K0302E4.
Stryker recalls specific end cap implants due to potential blister pack contamination. This could compromise sterility during surgery. Affected units have catalog number 18300015S and lot number K037E2D.
Stryker recalls single-use end cap implants due to potential blister pack contamination. Affected items have catalog number 18300005S and lot number K02803B. Consumers should contact Stryker for details.
Stryker recalls a specific locking screw implant due to potential blister pack compromise affecting sterility. This could lead to infection risks during surgery. Affected units have catalog number 18915055S.
Stryker recalls specific locking screws due to blister pack seal issues that may compromise sterility. Affected lots: K0207B3, K031B6B, K031B6C, K033439. Contact for replacement.
Stryker recalls End Cap, Std, Ti Gamma3 (Catalog 30051100S) due to potential blister pack seal compromise affecting sterility. This single-use medical device may not be sterile if the blister pack is damaged.
Stryker recalls End Cap T2 Tibia +10 mm implants (catalog 18220010S) due to potential blister pack seal failure, risking contamination during surgery.
Stryker recalls specific humerus screws due to potential blister pack contamination. Affected implants may not be sterile, risking infection after surgery.
Stryker recalls specific locking screws due to potential blister pack compromise affecting sterility. Affected lots include K029C38-K031B66. Contact Stryker for details.
Stryker recalls Advanced T2 Tibia Compression Screws (Catalog 18220001S) due to potential blister pack compromise affecting sterility. This single-use medical implant may not be sterile if the packaging is damaged.
Stryker recalls T2 Alpha Delta Strike Plate instruments due to potential breakage during nail procedures, which may cause complications. Affected units include specific model and lot numbers.
Stryker recalls a pin-to-rod coupling for fracture treatment. The device may not clamp pin and rod as intended, risking improper fixation. Affected units include specific model and lot numbers.
Stryker recalls Endotrac ECTR Triangle Blade (Catalog 2054A-1) due to potential compromised sterile bag seals. This could lead to infection risks during surgery. Affected units include Lot 01408.
Stryker recalls Endotrac ECTR Hook Blade (Catalog 2055A-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected patients should contact Stryker for details.
Stryker recalls Endotrac EPF/EGR Triangle Blade (Catalog 305:4A-1) due to potential compromised sterile bag seals. This could lead to infection risks during surgery. Affected units sold with lot number 01411.
Stryker recalls Endotrac ECTR Hook Blade (Catalog 2:055-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected units include specific lot numbers.
Stryker recalls Endotrac ECTR Triangle Blade (Catalog 2054-1) due to potential compromised sterile bag seals. This could lead to infection risks during plantar fasciosis treatment. Affected units sold with Lot 01407.
Stryker recalls Endotrac ECTR Push Blade (Catalog 2:053-1) due to potential compromised sterile bag seals. This could lead to infection risks during plantar fasciosis treatment. Affected units include Lot 01400.
Stryker recalls Endintrak 2 Hook Blade (Catalog 4058A-1) due to potential compromised sterile bag seals. This could risk infection during plantar fasciitis surgery. Affected units sold with lot numbers 01405 or 01479.
Stryker recalls Endotrac EPF/EGR Hook Blade (Catalog 3055A-1) due to potential compromised sterile bag seals. Affected units sold with Lot Number 01402 may pose infection risks if used.
Stryker recalls Endotrac EPF/EGR Triangle Blade (Catalog 305: 01398, 01465, 01481) due to potential compromised sterile bag seals. This could risk infection during surgery.
Stryker recalls Endintrak 2 Hook Blade (Catalog 4058-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected units sold with Lot 01412.
Stryker recalls Endotrac EPF/EGR Push Blade (catalog 305:1) due to potential compromised sterile bag seals. This could lead to infection risks during plantar fasciosis treatment. Affected lots: 01399, 01464, 01477.
Stryker recalls Endotrac EPF/EGR Hook Blade (Catalog 305:1) due to potential compromised sterile bag seals. This may risk infection during surgery. Affected lot numbers: 01403, 01466, 01483.
Stryker recalls Endotrig ETF Hook Blade (Catalog 1052-1) due to potential compromised sterile bag seals. This could risk infection during surgery. Affected lots: 01406, 01475.
Stryker recalls Endotrac ECTR Hook/Triangle Blade Kit (Catalogue 2:056-1) due to potential compromised sterile bag seals. Affected units sold with Lot # 01410. No specific remedy stated in recall notice.
Stryker recalls Endotrac EPF/EGR Hook/Triangle Blade Kit (Catalogue 3056-1) due to potential compromised sterile bag seals. Affected units include specific lot numbers. Consumers should contact Stryker for details.
Stryker recalls Basic T2 Femur Long Instrument Tray (lot K026ACE/KU97181) due to risk of using wrong instrument set during knee surgery. Affected users should verify model numbers.
Stryker recalls Hoffman LRF Hexapod Strut model 4935-0-010 due to potential pin displacement causing instability. Affected units sold in specific lots from 2016.
Stryker recalls Hoffman LRF Hexapod Struts with model 4935-0-030 due to potential pin displacement causing instability. Affected units sold in specific lots; contact for remedy.
Stryker recalls Hoffman LRF Hexapod Struts (Model 4935-0-020) due to potential pin displacement causing instability. Affected units sold in specific lots from 2016.
Stryker recalls Hoffman LRF Hexapod Struts with model 4935-0-040 due to potential pin displacement causing instability. Affected units sold in specific lots; contact Stryker for remedy.
Stryker recalls specific Hexapod software versions due to potential erroneous axial correction plans when creating correction plans with certain settings. Affected users should contact Stryker for details.
Stryker recalls specific ankle and humeral nail models due to potential sterility compromise from incomplete Tyvek lid seals. Affected items include right 10mm/200mm and 12mm/200mm ankle nails, and certain humeral nails. Contact Stryker for details.
Stryker recalls Farabeuf Clamp for 3.5mm Screws PRO (Catalog # 705463) due to laser etching on the wrong side of the lever arm. This could cause incorrect mode detection during use.
Stryker recalls certain Femoral Nails (A/R T2 Femur 12x360 mm) due to potential reduced strength causing premature breakage. Affected products have specific product numbers and lot codes.
Stryker recalls certain Femoral Nails (R150:12x380mm) due to potential reduced strength causing premature breakage. Affected products have specific product numbers and lot codes.
