The Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014in. The guidewires are compatible with existing microcatheters used in common procedures such as those used in endovascular diagnosis and therapy of neurovascular disease. The distal portion of the guidewire tip is radiopaque. For lubricity, the distal portion of the device is coated with a hydrophilic polymer and the proximal portion of the guidewire is coated with polytetrafluoroethylene (PTFE). The torque device included with the guidewire attaches to the proximal end of the wire and functions as a steering guide. Rotation of this device facilitates guidewire placement into the appropriate vessel by precise directional manipulation of the guidewire tip. The introducer included with the guidewire is intended to aid insertion of the guidewire into the catheter hub and/or hemostasis valve.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Catalog/UDI-DI/Lots: SSFT215PRE/07613327508598/0000139994, 0000144321, 0000146842, 0000154408; SSFT215STR/07613327508574/0000122897, 0000123151, 0000123405, 0000124931, 0000125040, 0000125719, 0000125720, 0000125787, 0000126356, 0000129220, 0000129221, 0000130861, 0000131723, 0000132954, 0000133179, 0000137045, 0000138580, 0000138581, 0000142280, 0000142281, 0000143349, 0000143584; SSFT300STR/07613327508581/0000144375, 0000155022; SSTD215PRE/07613327508512/0000122145, 0000122866, 0000127369, 0000139986, 0000140672, 0000141825, 0000141826, 0000143802, 0000146926, 0000149561, 0000154409, 0000154410, 0000154411, 0000176472; SSTD215STR/07613327508499/0000122481, 0000122485, 0000122650, 0000123069, 0000123070, 0000123143, 0000125409, 0000127494, 0000127495, 0000128254, 0000128446, 0000128447, 0000131661, 0000131667, 0000131668, 0000133396, 0000133563, 0000133564, 0000140971, 0000141392, 0000141393, 0000142532, 0000143125, 0000143209, 0000143806, 0000143834, 0000144140, 0000148427, 0000148428, 0000148477, 0000149560, 0000154679, 0000154680, 0000154681, 0000155021, 0000155662, 0000156792, 0000164588, 0000164589, 0000164591, 0000172898, 0000172899, 0000172900, 0000172911, 0000175987, 0000176018, 0000176019; SSTD300STR/07613327508505/0000145095, 0000145694, 0000151281; SSUP215PRE/07613327508635/0000144317, 0000148425; SSUP300PRE/07613327508642/0000145692, 0000151280; SSUP215STR/07613327508611/0000128253, 0000129625, 0000137050, 0000140671, 0000141784, 0000143342, 0000144318, 0000145693, 0000145875, 0000164662, 0000165477; SSUP300STR/07613327508628/0000121919, 0000141789, 0000145691
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Stryker Neurovascular
- Reason for Recall:
- Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backloading the guidewire through the optional introducer accessory. This issue is limited to certain lots of the Synchro Guidewire that contain an older version of the introducer accessory. Due to variation in the manufacturing process of the supplier of the introducer accessory, certain lots of introducers have sharper than intended edges that can peel off the PTFE coating when physicians use a technique known as backloading. Users with impacted product in their inventory are cautioned not to use this backloading technique.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
The Synchro SELECT Guidewires are a steerable guidewire family with a shapeable tip and are available in straight and pre-shaped versions. The outside diameters of the guidewires are 0.014in. The guidewires are compatible with existing microcatheters used in common procedures such as those used in endovascular diagnosis and therapy of neurovascular disease. The distal portion of the guidewire tip is radiopaque. For lubricity, the distal portion of the device is coated with a hydrophilic polymer and the proximal portion of the guidewire is coated with polytetrafluoroethylene (PTFE). The torque device included with the guidewire attaches to the proximal end of the wire and functions as a steering guide. Rotation of this device facilitates guidewire placement into the appropriate vessel by precise directional manipulation of the guidewire tip. The introducer included with the guidewire is intended to aid insertion of the guidewire into the catheter hub and/or hemostasis valve.
Product Codes/Lot Numbers:
Catalog/UDI-DI/Lots: SSFT215PRE/07613327508598/0000139994, 0000144321, 0000146842, 0000154408; SSFT215STR/07613327508574/0000122897, 0000123151, 0000123405, 0000124931, 0000125040, 0000125719, 0000125720, 0000125787, 0000126356, 0000129220, 0000129221, 0000130861, 0000131723, 0000132954, 0000133179, 0000137045, 0000138580, 0000138581, 0000142280, 0000142281, 0000143349, 0000143584; SSFT300STR/07613327508581/0000144375, 0000155022; SSTD215PRE/07613327508512/0000122145, 0000122866, 0000127369, 0000139986, 0000140672, 0000141825, 0000141826, 0000143802, 0000146926, 0000149561, 0000154409, 0000154410, 0000154411, 0000176472; SSTD215STR/07613327508499/0000122481, 0000122485, 0000122650, 0000123069, 0000123070, 0000123143, 0000125409, 0000127494, 0000127495, 0000128254, 0000128446, 0000128447, 0000131661, 0000131667, 0000131668, 0000133396, 0000133563, 0000133564, 0000140971, 0000141392, 0000141393, 0000142532, 0000143125, 0000143209, 0000143806, 0000143834, 0000144140, 0000148427, 0000148428, 0000148477, 0000149560, 0000154679, 0000154680, 0000154681, 0000155021, 0000155662, 0000156792, 0000164588, 0000164589, 0000164591, 0000172898, 0000172899, 0000172900, 0000172911, 0000175987, 0000176018, 0000176019; SSTD300STR/07613327508505/0000145095, 0000145694, 0000151281; SSUP215PRE/07613327508635/0000144317, 0000148425; SSUP300PRE/07613327508642/0000145692, 0000151280; SSUP215STR/07613327508611/0000128253, 0000129625, 0000137050, 0000140671, 0000141784, 0000143342, 0000144318, 0000145693, 0000145875, 0000164662, 0000165477; SSUP300STR/07613327508628/0000121919, 0000141789, 0000145691
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1940-2024
Related Recalls
Stryker Neurovascular has observed that devices with Out of United States (OUS) approved Instructions for Use (IFU) and Packaging Labels (pouch and carton), different configurations, have been erroneously distributed to customers in the US.
Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backloading the guidewire through the optional introducer accessory. This issue is limited to certain lots of the Synchro Guidewire that contain an older version of the introducer accessory. Due to variation in the manufacturing process of the supplier of the introducer accessory, certain lots of introducers have sharper than intended edges that can peel off the PTFE coating when physicians use a technique known as backloading. Users with impacted product in their inventory are cautioned not to use this backloading technique.
Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backloading the guidewire through the optional introducer accessory. This issue is limited to certain lots of the Synchro Guidewire that contain an older version of the introducer accessory. Due to variation in the manufacturing process of the supplier of the introducer accessory, certain lots of introducers have sharper than intended edges that can peel off the PTFE coating when physicians use a technique known as backloading. Users with impacted product in their inventory are cautioned not to use this backloading technique.