Every recall we track for Stryker Sustainability Solutions — 47 in all — plus the complaints and injury reports the public filed about them.
Stryker recalls BARD EP XT Steerable catheters with incomplete sterile seals that could lead to infections during medical procedures. Affected units include specific product numbers and lot numbers.
Stryker recalls BARD Dynamic Tip Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Stryker recalls BARD Dynamic XT Deca Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units have specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units include specific lot numbers and product codes.
Stryker recalls CS Uni-Directional w Auto ID catheters with Product Number D135303 due to incomplete sterile seals. Affected units include specific lot numbers. Stop using immediately to prevent infection risks.
Stryker recalls BARD Dynamic XT Steerable catheters with incomplete sterile seals that could lead to infections during medical procedures. Affected units have specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units have specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Stryker recalls BARD Dynamic XT Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units include specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infections during medical procedures. Affected units include specific product numbers and lot codes.
Stryker recalls Medtronic Marinr Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infections during medical procedures. Affected units have specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals. These reprocessed electrophysiology catheters may not be sterile, risking infection during procedures.
Stryker recalls BW Webster Duo-Decapolar electrophysiology catheters with incomplete sterile seals. Affected units have specific product numbers and lot numbers. Stop using immediately to prevent infection risks.
Stryker recalls CS Uni-Directional w Auto ID catheters (Product Number D135304) with incomplete sterile seals. Check UDI 07613327357318 and Lot Numbers listed for affected units. Stop using if you have this model.
Stryker recalls Daig Livewire Steerable BDB catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Stryker recalls BARD Dynamic Tip Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units include specific product numbers and lot numbers listed in the recall notice.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could compromise safety during medical procedures. Affected units have specific product numbers and lot codes.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to infections during medical procedures. Affected units include specific product numbers and lot codes.
Stryker recalls BARD EP XT Decapolar Steerable catheters with incomplete sterile seals. This may cause infections during medical procedures. Affected units have specific product numbers and lot numbers listed in the recall.
Stryker recalls Daig Livewire Steerable catheters with incomplete sterile seals that could lead to contamination during medical procedures. Product numbers and lot numbers listed in the recall.
Stryker recalls BARD Dynamic Deca Steerable catheters with incomplete sterile seals that could lead to infection during medical procedures. Affected units have specific UDI and lot numbers listed in the recall notice.
Stryker recalls BARD Dynamic Tip Steerable catheters with incomplete sterile seals that could compromise infection control. Affected units include specific lot numbers and product numbers.
Stryker recalls 18" and 24" yellow/red color cuffs with potential detachment at welding connection, causing pressure loss. Affected units include specific serial numbers.
Stryker recalls reprocessed Harmonic Focus Shears with Adaptive Tissue Technology that may become stuck in the 'on' position, causing continuous activation. Affected units have specific lot numbers and were sold for single-use procedures.
Stryker recalls disposable 5 lead cable and lead wire systems that may contain reprocessed ECG leads not approved for reuse, potentially causing device malfunction.
Stryker recalls blue 30" tourniquet cuffs labeled as dual port but contain single port. Check packaging for model number 60-7070-0:005 to avoid confusion.
Stryker recalls BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters (REF D134301) due to failing electrophysiology testing requirements. Affected units have specific serial numbers and UDI codes.
Stryker recalls HoverMatt mattresses with incorrect width that may cause increased skin tears during patient transfers. Affected units were sold between November 28 and December 8, 2022. Contact Stryker for details.
Stryker recalls DVT compression foot covers that may be mislabeled or mispackaged. This could lead to incorrect medical use. Affected items have specific lot numbers and sizes.
Stryker recalls specific Color Cuff tourniquet cuffs that may tear or have faulty O-rings, causing pressure loss and potential bleeding during medical procedures.
Stryker recalls 18" Red Color Cuff (Quick Connect Single Port) due to mislabeling as single-bladder when it's dual-bladder. This could lead to improper use in medical settings.
Stryker recalls Harmonic ACE +7 Shears with Advanced Hemostasis due to distribution without regulatory clearance. Affected units include specific model and lot numbers. Consumers should contact Stryker for details.
Stryker recalls certain Cardiovascular Reprocessed ViewFlex Xtra ICE Catheters with incorrect expiration dates that may cause sterility breaches or treatment delays. Affected units have a one-year shelf life but are labeled as two years.
Stryker recalls blue 30" Zimmer tourniquet cuffs with potential mislabeling that could cause improper use or inadequate limb compression during procedures.
Stryker recalls BW Lasso 2515 ANV eco Variable Diagnostic EP Catheters with specific lot codes due to potential EEPROM chip errors when used with CARTO EP Navigation Systems.
Stryker recalls eco reprocessed electrophysiology catheters (item # D134903) that are not approved for reprocessing, which could lead to improper use.
Stryker Sustainability Solutions recalls reprocessed arthroscopic shavers with specific catalog numbers that may display incorrect settings or error messages when connected to generators, potentially affecting surgical use.
Stryker recalls reprocessed Xcel Bladeless Trocars (H12LP) distributed after a prior recall. These endoscopic surgical tools may be in use at medical facilities. No specific remedy is stated in the recall notice.
Stryker recalls reprocessed HARMONIC Ace+7 shears that may show 'No Instrument Uses Remaining' error code, preventing use. Affected units may need replacement.
Stryker Sustainability Solutions recalls two specific Coronary Sinus Uni-Directional Diagnostic EP Catheter models (D135303/D135304) due to failing non-thrombogenic specifications in testing. The catheters are used for cardiac electrophysiology mapping.
Stryker recalls reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters due to potential EEPROM chip errors when used with CARTO EP Navigation Systems. Affected units have specific serial numbers.
Stryker recalls reprocessed BW Lasso 2515 NAV eco Variable Diagnostic EP Catheters due to potential EEPROM chip errors when used with CARTO EP Navigation Systems version 2.3 or higher.
Stry: 3040-VenaFlow Calf Garment (Aircast) was mislabeled as 3010-PL Aircast Pos-Lock Connector. This could cause confusion with a different product intended for DVT prevention. Affected units have UDI: 00885825016661.
