Recall Z-2201-2012 ยท GZT Retractor, Self-Retaining, For Neurosurgery
Nico Corp.
13.5 mm x 60 mm BrainPath Sheath The NICO BrainPath is a family of products that consists of multiple sized reusable and re-sterilizable obturators with coordinating single patient use, disposable sheaths (three lengths available for each: 50mm, 60mm, and 75mm). The obturator and sheath are assembled in the OR immediately prior to use. These two components are held together by an interference fit
| Date | Aug 13, 2012 (initiated Jul 17, 2012) |
| Status | Terminated |
| Reason | BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled as 60mm. The length callout on the label does not match the actual length of the sheath within the packaging resulting in an improper fit as further explained below. This mislabeling was discovered on 29-June-2012 during a clinical case. |
| Root cause | Labeling mix-ups |
| Action | NICO Neuro and Spine sent an Urgent Recall letter to all affected customers on July 18, 2012. The letter identified the product, the problem, and the action to be taken by the customer. Customers were asked to complete the recall response form. Affected sheaths distributed within the US will be obtained and discarded by NICO. Affected sheaths shipped to Canada will be obtained and discarded by NICOs distributor, Galen Medical. For questions customers should call 888-632-7071. |
| Quantity | 15 devices (3 boxes, 5 devices per box) |
| Distribution | Worldwide Distribution - USA including MI and Canada |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K120691 | BRAIN PORT Nico Corporation, Jun 5, 2012 |