Shoreside Enterprises Inc.

FDA Regulatory Profile

Shoreside Enterprises Inc. appears in FDA public data with 2 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0880-2018, Class I) was initiated on May 17, 2018.

Summary

Total Recalls
2 (2 Class I)
510(k) Clearances
0
Inspections
2
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0880-2018Class I7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, May 17, 2018
D-0879-2018Class IPOSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed bMay 17, 2018