Medical DeviceSep 5, 2018
Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing recall — FDA Z-2948-2018
Packaged with an incorrect overwrap.
Class IIFDA: TerminatedMedline Industries Inc.
Recall history in this database
Classification mix: Class II: 133, Class III: 2, Class I: 2.
Medical DeviceJun 6, 2018
MEDLINE Sterile* Needle Counter, 40Ct recall — FDA Z-1932-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceJun 6, 2018
MEDLINE O.R. Necessities(R) STERILE R, Needle Counter/Compte-aiguiles/Caja de agujas, Gold recall — FDA Z-1936-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceJun 6, 2018
MEDLINE O.R. Necessities(TM) Sterile* Needle Counter, 100 Ct. Double Magnet / Foam Block recall — FDA Z-1934-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceJun 6, 2018
MEDLINE O.R. Necessities(TM) Sterile* Needle Counter, 40 Ct. Double Magnet / Foam Block with recall — FDA Z-1935-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceJun 6, 2018
MEDLINE Sterile* Needle Counter, 40Ct recall — FDA Z-1933-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
Medical DeviceJun 6, 2018
MEDLINE Sterile* Needle Counter, 100Ct recall — FDA Z-1931-2018
The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle…
Class IIFDA: TerminatedMedline Industries Inc.
DrugMar 7, 2018
POVIDONE-IODINE PVP Scrub Solution, Povidone Iodine, 7.5% recall — FDA D-0546-2018
Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.
Class IIFDA: TerminatedMedline Industries Inc.
DrugFeb 7, 2018
Medline Suture Removal Tray recall — FDA D-0264-2018
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 General Purpose Kit, Sterile, Single use only recall — FDA D-0271-2018
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 Vitrectomy CDS Pack, Single Use Only recall — FDA D-0255-2018
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 IV Start Kit, Sterile, Single Use Only recall — FDA D-0298-2018
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 Vaginal Delivery CDS Pack, Single Use Only recall — FDA D-0254-2018
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 Dressing Change Tray Kit, Sterile, Single use only recall — FDA D-0273-2018
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.
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 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 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
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 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 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
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
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 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.
Understanding this recall history
This page summarizes recall records in which the official source identifies Medline Industries, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.