TESTOSTERONE, Pellet, 125 mg, Rx only, JD & SN Inc, DBA Moses Lake Professional Pharmacy, 1555 S. Pilgrim St. Moses Lake WA 98837, (509)764-2314

Recall Insight

This FDA Drug action (record #D-0132-2016) was formally reported on November 4, 2015, with the manufacturer initiating the action on July 24, 2015. It is classified under Moderate severity (Class II), with a current status of Terminated. JD & SN Inc., dba Moses Lake Professional Pharmacy is listed as the recalling firm, operating out of Moses Lake, WA. Federal records indicate 355 pellets units are affected.

The documented reason for this recall is: Lack of Assurance of Sterility; all sterile human compounded drugs within expiry Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 5 were also issued by FDA Drug. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 11 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.