CGMP Deviations; deficiencies observed during FDA inspection
Reason for recall: CGMP Deviations; deficiencies observed during FDA inspection Distribution: US Nationwide. Quantity: 4,738 tubes Lot/code info: Lot# 003, 004, 005, 006, 007, 008, 009, 010, 011, 012, 014, 015, 017, 018, 019, 020, 021, 022, 023, 024, 025, 026, 027, 028, 029, 030, 034, 035, 036, 037, 038, 039, 041, 042, 043, 044, 048, 049, 050, 051, 052, 053, 054, 055, 056, 057, 058, 059, 060, 061, 062, 063, 064, Within Expiry.
Official record: FDA (Drug enforcement) ↗
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