Medline Industries Recalls 45 Tracheostomy Tube Kits Over Labeling Discrepancy
The FDA has classified the recall as Class II, indicating the product may cause temporary or medically reversible harm.
Recalls & Safety Alerts in Northfield, Illinois
Every recalls & safety alerts report published for Northfield, Illinois, newest first.
FDA Closes Medline Neuro Kit Recall Over Endotoxin Levels
The FDA has terminated its enforcement action on 3,468 Medline neurological convenience kits recalled for potential out-of-specification endotoxin levels in the neurosponges they contain.
Medline Recalls 663 Surgical Convenience Kits Over Potentially Contaminated Component
The FDA has classified the recall of 14 Medline convenience kit lines as Class II, meaning the product may cause temporary or medically reversible harm.
Medline recalls 15 convenience kits over potentially contaminated component
FDA classifies the action as Class II, saying the chance of serious harm is remote.
Medline recalls 419 surgical convenience kits over potentially contaminated component
FDA lists action as Class II recall; kits contain a component recalled by the manufacturer.
FDA closes recall of Medline neonatal breathing circuits
The agency has closed the Class II recall of certain heated wire breathing circuits distributed by Medline Industries, LP.
FDA closes recall of Medline neonatal heated breathing circuits
The agency has closed the Class II recall of Medline Hudson RCI heated wire breathing circuits, citing completion of the corrective action.
FDA closes recall of Medline surgical kits over potentially contaminated component
The agency considers the recall carried out; consumers are urged to check the listed lot numbers.
Medline Recalls Bleach Wipes Over Reduced Disinfectant Strength
FDA classifies recall of Medline Micro-Kill Bleach Germicidal Wipes as Class II due to potential loss of bleach concentration before shelf life ends.
Medline Recalls Bleach Wipes Over Reduced Disinfectant Strength
FDA classifies the action as Class II, citing a potential drop in bleach concentration below specification before the labeled shelf life ends.
Medline Recalls 980 Prostate Procedure Kits Over Recalled Bard Foley Catheters
An FDA enforcement report classifies the ongoing action as Class II, the agency's middle category.
FDA Records Class II Recall of 980 Medline Prostate Pack Kits Over Bard Foley Catheters
An FDA enforcement report lists an ongoing recall by Medline Industries, LP of convenience kits containing recalled Bard Silastic Foley catheters, distributed in five states.
FDA Records Class II Recall of 980 Medline Catheter Kits
An FDA enforcement report filed under recall number Z-2782-2026 lists 980 Medline convenience kits containing Bard Silastic Foley catheters, with the recall status ongoing.
FDA Classifies Recall of 60 Medline Anterior Hip Surgical Kits as Class I
The agency's enforcement report for recall Z-2747-2026 traces the action to a voluntary recall of a bupivacaine injection supplied within the kits.
FDA Records Class II Recall of 980 Medline Catheter Kits Over Bard Silastic Foley Catheters
The enforcement record cites an increased amount of raw material on the catheter surface; the action is listed as ongoing.
Medline Recalls 1,601 Surgical Convenience Kits Over Possible Bacillus Contamination
An FDA enforcement report lists nine kit types containing BD PurPrep 26 mL as Class II, with the recall still ongoing.
Medline Recalls 980 Urology Kits Containing Recalled Bard Foley Catheters
An FDA enforcement report lists the Class II action as initiated June 8, 2026 and still ongoing.
Medline Recalls 980 Urology Procedure Kits Over Bard Silastic Foley Catheters
An FDA enforcement report lists the Class II recall as ongoing, covering kits distributed nationwide with catheters recalled by their manufacturer over raw material on the catheter surface.
Medline Recalls 398 Surgical Convenience Kits Over Possible Contamination in Antiseptic Component
An FDA enforcement report lists the recall as Class II and ongoing, covering shoulder and major orthopedic packs distributed in ten states.
FDA Classifies Recall of 318 Medline Surgical Kits as Class I
Enforcement report Z-2765-2026 says the knee and hip procedure kits contain recalled ICU Medical pain management kits with Bupivacaine Hydrochloride in Dextrose Injection, USP.