DrugFeb 7, 2018
Medline Concordia Nurse Bag Kit recall — FDA D-0259-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
Monthly breakdown
2018 recalls by month
Select a month to review the recall records reported during that period.
December 2018285 records · 4 categoriesNovember 2018342 records · 4 categoriesOctober 2018626 records · 4 categoriesSeptember 2018393 records · 4 categoriesAugust 2018569 records · 4 categoriesJuly 2018356 records · 4 categoriesJune 2018402 records · 4 categoriesMay 2018613 records · 4 categoriesApril 2018449 records · 3 categoriesMarch 2018523 records · 3 categoriesFebruary 2018612 records · 3 categoriesJanuary 2018290 records · 3 categories
2018 recalls — page 215
Records are ordered by the best available source date.
DrugFeb 7, 2018
Medline INCISION AND DRAINAGE TRAY Kit, Sterile, Single use only recall — FDA D-0274-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Debridement Tray, Sterile, Single Use Only recall — FDA D-0300-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Industries Professional Hospital Supply Suture Removal Kit, Sterile, Single Use Only recall — FDA D-0311-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0292-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline RAD NECK ENT TRAY Pack, Single Use Only recall — FDA D-0256-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0317-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0287-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Johnson & Johnson Neutrogena deep clean purifying whipped foam cleanser recall — FDA D-0244-2018
Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.
Class IIFDA: TerminatedJohnson & Johnson
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0285-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal LIEN CHAN FOR SEVEN DAYS capsules, labeling is in foreign language recall — FDA D-0570-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
Medline Pediatric IV Kit recall — FDA D-0260-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Industries Aplicare Povidone-Iodine Prep Pad, Antiseptic, Sterile Solution, Active recall — FDA D-0252-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal GERMANY BLACK GOLD tablets, 2800 mg, 8-count bottle, labeling is in foreign recall — FDA D-0555-2018
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Class IFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
BLUE PEARL capsules, 500mg, 1-count packets recall — FDA D-0247-2018
Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making this an…
Class IFDA: TerminatedBlue Fusion Natural
DrugFeb 7, 2018
Medline Incision and Drainage Tray Kit, Sterile, Single use only recall — FDA D-0267-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
A&H Focal Indian God Lotion Spray Bottle, labeling is in foreign language recall — FDA D-0553-2018
Marked Without An Approved NDA/ANDA: FDA analysis found this product to contain diethyl phthalate, an inactive ingredient in several modified release solid oral dosage forms, making this…
Class IIIFDA: TerminatedA&H Focal Inc.
DrugFeb 7, 2018
Medline Suture Removal Kit, Sterile, Single Use Only recall — FDA D-0294-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Incision Drainage Tray, Sterile, Single Use Only recall — FDA D-0315-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Central Line Dressing Change Tray Kit, Sterile, Single use only recall — FDA D-0266-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Oxycodone Hydrochloride Tablets, USP 15 mg, 100 count bottles recall — FDA D-0248-2018
Labeling; Label Error Not Elsewhere Classified; label missing controlled substance CII symbol
Class IIIFDA: TerminatedAscent Pharmaceuticals, Inc.
DrugFeb 7, 2018
Medline General Purpose Instrument Set, Sterile, Single Use Only recall — FDA D-0295-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Abdominal Surgery II Pack-LF, Sterile, Single Use Only recall — FDA D-0316-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray, Sterile, Single Use Only recall — FDA D-0284-2018
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Class IIFDA: TerminatedMedline Industries Inc.
About the 2018 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.