DrugSep 21, 2022
MAGNESIUM CITRATE P, magnesium citrate SALINE LAXATIVE, Oral Solution, (1.745 g/fl oz) recall — FDA D-1505-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
Latest records
Latest recalls — page 332
The newest recall records with useful source details are listed here.
DrugSep 21, 2022
Pine Pharmaceuticals Bupivacaine HCl 0.375% w/v and Lidocaine HCl 2% w/v Solution for recall — FDA D-1514-2022
Lack of Assurance of Sterility
Class IIFDA: TerminatedPine Pharmaceuticals, LLC
DrugSep 21, 2022
MAGNESIUM CITRATE Kroger, Magnesium Citrate SALINE LAXATIVE, Oral Solution, 1.745 g, Lemon recall — FDA D-1503-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
PROPOFOL Injectable Emulsion, 1 g/100 mL (10 mg/mL) recall — FDA D-1540-2022
Presence of particulate matter
Class IFDA: TerminatedPfizer Inc.
DrugSep 21, 2022
RemedyRepack Lisinopril 10 mg tablets, 30-count Blister Card recall — FDA D-1538-2022
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Class IIFDA: TerminatedRemedyRepack Inc.
DrugSep 21, 2022
Vi-Jon Walgreens, Dye-Free, Magnesium Citrate, SALINE LAXATIVE, Oral Solution recall — FDA D-1509-2022
Microbial contamination of non-sterile products.
Class IFDA: TerminatedVi-Jon, LLC
DrugSep 21, 2022
Lisinopril Tablets USP, 10 mg, 1000-count bottles recall — FDA D-1536-2022
Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleSep 19, 2022
Audi Q3 glass, side/rear recall — NHTSA campaign 22V701000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022 Audi Q3 vehicles. A window manufacturing error may allow the rear window to crack or break.
glass, side/rearVolkswagen Group of America, Inc.
VehicleSep 19, 2022
Tesla power window devices and controls recall — NHTSA campaign 22V702000
Tesla, Inc. (Tesla) is recalling certain 2017-2022 Model 3, 2020-2022 Model Y, and 2021-2022 Model S and Model X vehicles. The window automatic reversal system may not react correctly after…
power window devices and controlsTesla, Inc.
VehicleSep 19, 2022
Kia trailer hitch recall — NHTSA campaign 22V703000
Kia America, Inc. (Kia) is recalling certain 2016-2022 Sorento, 2021-2022 Sorento Hybrid (HEV), 2022-2023 Sorento Plug-In Hybrid (PHEV), and 2017-2022 Sportage vehicles equipped with a tow…
trailer hitchKia America, Inc.
DrugSep 14, 2022
Plastikon Healthcare GUAIFENESIN AND DEXTROMETHORPHAN 200-20 mg/10 mL, 10 mL cup recall — FDA D-1491-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare Magnesium Hydroxide 2400 mg, Aluminum Hydroxide 2400 mg, Simethicone recall — FDA D-1479-2022
Microbial Contamination of Non-Sterile Products.
Class IFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare GUAIFENESIN AND DEXTROMETHORPHAN 100 mg-10 mg/5 mL, 5 mL cup recall — FDA D-1490-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare CORRECTDOSE Children's COUGH & CHEST CONGESTION DM recall — FDA D-1494-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup recall — FDA D-1480-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare CORRECTDOSE Children's ALLERGY RELIEF recall — FDA D-1492-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle recall — FDA D-1499-2022
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Class IIFDA: TerminatedCIPLA
DrugSep 14, 2022
Plastikon Healthcare MILK OF MAGNESIA USP, 2400 mg/30 mL, Magnesium Hydroxide, 30 mL cup recall — FDA D-1476-2022
Microbial Contamination of Non-Sterile Products
Class IFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone recall — FDA D-1482-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Akorn Sodium Chloride Ophthalmic Ointment USP, 5%, Sterile, Net Wt 3.5 g (1/8 oz) tube, Mfg recall — FDA D-1496-2022
cGMP Deviations: Turbidity discovered in Artificial Tears Ointment during sterility testing. Scope expanded to include other lots and products which potentially share the same root cause.
Class IIFDA: TerminatedAkorn, Inc.
DrugSep 14, 2022
CIPLA Difluprednate Ophthalmic Emulsion, 0.05%, 5 mL bottle recall — FDA D-1498-2022
Lack of Assurance of Sterility: customer complaint for defective container where breakage of the protective cap exposes tip of eye drop which could compromise sterility.
Class IIFDA: TerminatedCIPLA
DrugSep 14, 2022
Plastikon Healthcare CALCIUM CARBONATE ORAL SUSPENSION, 1250 mg/5 mL, 5 mL cup recall — FDA D-1487-2022
CGMP Deviations: products manufactured under conditions which reflect manufacturing processes that were not adequately controlled.
Class IIFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare Magnesium Hydroxide 1200 mg, Aluminum Hydroxide 1200 mg, Simethicone recall — FDA D-1478-2022
Microbial Contamination of Non-Sterile Products.
Class IFDA: TerminatedPlastikon Healthcare LLC
DrugSep 14, 2022
Plastikon Healthcare MILK OF MAGNESIA USP, 2400 mg/10 mL, Magnesium Hydroxide, 30 mL cup recall — FDA D-1477-2022
Microbial Contamination of Non-Sterile Products.
Class IFDA: TerminatedPlastikon Healthcare LLC
Browse by month
Recent recall archives
Browse recent months with enough recall history for useful comparison.
August 2026149 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categories