Dabur India Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin recall — FDA D-0642-2026
CGMP Deviations; deficiencies observed during FDA inspection
Complete FDA and NHTSA recall records dated in June 2026.
These records include useful source details for the selected month.
CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
CGMP Deviations; deficiencies observed during FDA inspection
Defective container:may contain bottles with incomplete seals
Failed Dissolution Specifications
CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
CGMP Deviations; deficiencies observed during FDA inspection
Defective container:may contain bottles with incomplete seals
Undeclared Allergen (Soy)
Products were made with recalled California Dairies milk powder due to Salmonella.
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
The product contains unapproved colors chlorophyll E140 and E141.
Undeclared fish.
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
Undeclared melatonin.
The product contains unapproved colors chlorophyll E140 and E141.
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.