Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape.
Reason for recall: Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were distributed with a tip curve shape which differs from the labeled tip curve shape. Distribution: US Nationwide distribution in the state of Indiana. Quantity: 116 units Lot/code info: GTIN 08714729283546, Lot/Batch Numbers: 25715222, 27762225, 27780464
08714729283546
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.