Stryker Corporation

Stryker Neurovascular's INZONE Detachment System devices may experience premature battery drain, causing them to fail to power on, display faint indicators, or be unable to detach an embolization coil as intended. If a device fails during a procedure, medical staff may need to use an alternative technique to complete the intervention.

Medtronic discovered that certain lots of the Marinr Steerable reprocessed electrophysiology catheter have incomplete seals on the sterile packaging. This affects 87 units distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable BDB electrophysiology catheters (Product Number 401918) due to incomplete seals on the sterile packaging. This affects 2 units with specific lot numbers. Incomplete seals may allow contamination of the sterile product.

Stryker Sustainability Solutions issued a recall of Daig Livewire Steerable reprocessed electrophysiology catheters (Product Number 401932) due to incomplete seals on the sterile packaging. The incomplete seals could potentially allow contamination of the sterile product. A total of 458 units across multiple lot numbers were affected and distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions identified incomplete seals on certain lots of the Daig Livewire Steerable reprocessed electrophysiology catheter (Product Number 401923). The affected units may not maintain sterility, which could pose a risk during use. Three units have been affected.

Stryker Sustainability Solutions identified incomplete seals on certain lots of Daig Livewire Steerable electrophysiology catheters. The incomplete seals may compromise sterility of the product. Approximately 206 units across multiple lot numbers were affected.

Stryker Sustainability Solutions recalled Daig Livewire Steerable electrophysiology catheters (Product Number 401914) due to incomplete seals on the sterile packaging. The defect affects 10 units across 10 lot numbers distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling Daig Livewire Steerable electrophysiology catheters (Product Number 401908) due to incomplete seals on the sterile packaging. This affects 3 units with specific lot numbers distributed in the US, Canada, and Israel. Incomplete seals could allow contamination of the sterile product.

Stryker Sustainability Solutions is recalling certain lots of the Daig Livewire Steerable electrophysiology catheter because some units have incomplete seals on their sterile packaging. This affects 107 catheters distributed in the U.S., Canada, and Israel. No injuries have been reported.

Certain lots of the Daig Livewire Steerable electrophysiology catheter have incomplete seals on the sterile packaging. This could allow contamination of the device before use. The issue affects specific lot numbers of product number 401904.

Stryker Sustainability Solutions recalled certain reprocessed electrophysiology catheters (Daig Livewire Steerable, Product Number 401652) because the sterile packaging has incomplete seals. An incomplete seal can allow contamination to enter the package, compromising sterility before the device is used.

Stryker Sustainability Solutions identified incomplete seals on sterile packaging for certain Daig Livewire Steerable electrophysiology catheters. This affects 9 units distributed in the US, Canada, and Israel. No injuries have been reported.

Incomplete seals on sterile product

Stryker Sustainability Solutions recalled Daig Livewire Steerable electrophysiology catheters (Product Number 401581) because some units have incomplete seals on their sterile packaging. This affects 108 catheters distributed in the US, Canada, and Israel across multiple lot numbers.

Stryker Sustainability Solutions identified incomplete seals on certain lots of Daig Livewire Steerable reprocessed electrophysiology catheters. The seal defect could allow contamination of the sterile product. Affected units were distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling certain lots of CS Uni-Directional electrophysiology catheters (Product Number D135304) because some units have incomplete seals on their sterile packaging. An incomplete seal could allow the sterile catheter to become contaminated before use.

Stryker Sustainability Solutions' CS Uni-Directional w Auto ID electrophysiology catheter (Product Number D135303) has incomplete seals on some units, which could compromise sterility. The affected lots were distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling certain lots of the BW Webster Duo-Decapolar reprocessed electrophysiology catheter due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the sterile product before use. A total of 154 units were affected across the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling BARD EP XT Steerable electrophysiology catheters (Product Number 200794) due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the sterile device before use. A total of 44 units across multiple lot numbers have been affected.

Stryker Sustainability Solutions is recalling BARD EP XT Decapolar Steerable electrophysiology catheters (Product Number 201007) due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the catheter before use. A total of 217 units across multiple lot numbers were distributed in the U.S., Israel, and Canada.

Stryker Sustainability Solutions is recalling certain reprocessed BARD Dynamic XT Steerable electrophysiology catheters due to incomplete seals on the sterile packaging. The incomplete seals may allow contamination of the sterile product before use. This affects 5 units in the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling the BARD Dynamic XT Steerable electrophysiology catheter (Product Number 201103) due to incomplete seals on the sterile packaging. This defect could compromise the sterility of the device. The recall affects specific lot numbers distributed nationwide in the US, as well as in Israel and Canada.

Stryker Sustainability Solutions is recalling BARD Dynamic XT Deca Steerable electrophysiology catheters (Product Number 201102) due to incomplete seals on the sterile packaging. The defect affects 90 units across multiple lot numbers distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling the BARD Dynamic Tip Steerable catheter (Product Number 6DYNTP001) because some units have incomplete seals on their sterile packaging. This affects 427 units distributed in the US, Canada, and Israel. No injuries have been reported.

Stryker Sustainability Solutions is recalling BARD Dynamic Tip Steerable reprocessed electrophysiology catheters (Product Number 200344) due to incomplete seals on the sterile packaging. The incomplete seals could allow contamination of the sterile device. Affected lot numbers are listed by Stryker, and the recall impacts 28 units distributed in the US, Canada, and Israel.

Stryker Sustainability Solutions is recalling reprocessed BARD Dynamic Tip Steerable electrophysiology catheters (Product Number 200131) due to incomplete seals on the sterile packaging. The incomplete seals may compromise sterility, potentially allowing contamination of the device. Affected lot numbers span from 3966097 to 4762686, with 61 units distributed across the United States, Canada, and Israel.

Stryker Sustainability Solutions has recalled BARD Dynamic Deca Steerable electrophysiology catheters (Product Number 201101) due to incomplete seals on the sterile packaging. The affected catheters may not maintain sterility, which could pose a risk to patients. Approximately 3,063 units in multiple lot numbers are included in this recall.

Stryker Corporation recalled a limited lot of FluidSmart Urology Tube Sets (REF LL0006) used with fluid management systems in surgical procedures. Some units in this lot did not meet manufacturing standards. No injuries have been reported.

Due to potential for tourniquet cuffs to detach from the bladder at the welding connection and result in the cuff not being able to maintain pressure.

The surgical light assembly in Stryker CHROMOPHARE Softlit Ring systems may not adequately support the weight of the ceiling cover. This could potentially cause the cover to fall. No injuries have been reported.