Line Powered RePak, Model Number 1785S Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Line Powered RePak, Model Number 1785S
Lot Codes / Batch Numbers
Line Powered RePaks, Model Number 1785S, distributed from April 9, 2003 to May 7, 2003 are to be recovered. Between 04/09/03 and 05/07/03, 618 Line Powered RePaks (Model 1785S) were shipped.
Products Sold
Line Powered RePaks, Model Number 1785S, distributed from April 9, 2003 to May 7, 2003 are to be recovered. Between 04/09/03 and 05/07/03, 618 Line Powered RePaks (Model 1785S) were shipped.
A medical device manufacturer is recalling Line Powered RePak, Model Number 1785S due to If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If there was a short, excessive heat could have been generated in the transformer due to the use of the wrong fuse.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026