Recall Z-2765-2016 ยท GDF Guide, Needle, Surgical
Hologic, Inc
SureSight Obturator Introducer Localization Systems (ILS) for ATEC in MRI. ILS-0914-20-OB (9G Introducer Localization Set (OB Model) for ATEC0914-20MR Handpiece)
| Date | Sep 8, 2016 (initiated Aug 2, 2016) |
| Status | Terminated |
| Reason | Tip Breakage at the glue joint between the obturator body and tip |
| Root cause | Process control |
| Action | Hologic sent an Important Product Recall letter to customers in the United States through Certified letter. The letter identified the affected product, problem and actions to be taken. Customers were instructed to immediately examine their inventory and cease use of all affected recalled product. Customers were asked to complete the enclosed Recall Response Card indicating whether you have any of the recalled product on hand, as well as the quantity of product that you have in stock. |
| Quantity | 1440 units |
| Distribution | US Nationwide Distribution |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.