Recall Z-1482-2019 ยท HTW Bit, Drill
Zimmer GmbH
Drill, cannulated, 3x90mm, AO, Item Number ST502015631
| Date | Apr 8, 2019 |
| Status | Terminated |
| Reason | An investigation identified that the products were possibly manufactured from a different material than defined in the applicable specifications. |
| Root cause | Under Investigation by firm |
| Action | Urgent Medical Device Recall notification letters dated 4/8/19 were sent to customers. |
| Distribution | The products were distributed to the following US states: AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and WY. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.