Recall Z-0931-03 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
Rehabilicare
Line Powered RePak, Model Number 1785S
| Date | Jun 17, 2003 (initiated May 23, 2003) |
| Status | Terminated |
| Reason | If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse. |
| Root cause | Other |
| Action | Recall letters dated May 21, 2003 requested that consignees return the product and a response form to the firm. Distributors were requested to recall the product from their customers. |
| Quantity | 618 Line Powered RePaks |
| Distribution | Nationwide in the United States |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.