Manufacturer
351 recalls in our database name Medline Industries, LP as the manufacturing or recalling firm.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Medline Industries is recalling NERVE BLOCK TRAY 2 kits (SKU DYNJRA2713) due to complaints that butyrate tubing cracks during use of MASTISOL Liquid Adhesive. Affected kits should not be used.
Medline Industries recalls 117 surgical procedure kits nationwide due to defective MASTISOL adhesive vials. The tubing in the vials cracks during use, potentially affecting surgical procedures.
Medline Industries recalls 456 surgical procedure kits nationwide due to MASTISOL liquid adhesive with tubing that cracks when actuated. No illnesses have been reported.
Medline is recalling three types of medical procedure kits containing MASTISOL liquid adhesive with defective tubing that cracks during use. Approximately 1,928 units were distributed nationwide.
Medline Industries is recalling 1,928 circumcision procedure kits due to cracked tubing in the included MASTISOL liquid adhesive. The defect occurred during actuation of the adhesive vials.
Medline medical procedure kits are being recalled due to complaints that butyrate tubing cracks during actuation of MASTISOL Liquid Adhesive vials. The kits are distributed nationwide.
Medline is recalling multiple medical procedure convenience kits containing MASTISOL liquid adhesive because the butyrate tubing cracks during use, posing a potential safety risk. The recall affects 66 units distributed nationwide.
Medline Industries is recalling 1,928 units of two procedure convenience kits due to MASTISOL liquid adhesive vials with tubing that can crack during actuation, potentially affecting proper kit function.
Medline recalled multiple medical procedure kits due to a defect causing butyrate tubing in MASTISOL liquid adhesive vials to crack during use. The affected kits are used in neurological and surgical procedures.
Medline C-section procedure kits are recalled because the MASTISOL liquid adhesive they contain has butyrate tubing that cracks during use.
Medline Industries is recalling 1,928 medical procedure kits distributed nationwide. The kits contain MASTISOL liquid adhesive with defective butyrate tubing that cracks during activation.
Medline Industries is recalling Full Electric Lightweight Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions and pose a risk of fire.
Medline is recalling 13,245 Semi Electric Lightweight Homecare Beds because hand control pendants may overheat and pose a fire risk in certain conditions. The company has received 58 reports of pendant sparking, burning, melting, smoking, or fire.
Medline is recalling Full Electric Low Basic Homecare Beds due to a fire hazard in the hand control pendant. The pendant may overheat under certain operating conditions, creating a risk of fire.
Medline Industries recalls homecare beds due to fire risk in the hand control pendant. The pendant may overheat and ignite, posing a fire hazard to users.
Medline is recalling 373,392 Semi Electric Basic Homecare Beds due to hand control pendants that may overheat and pose a fire risk. The company has received 58 complaints of pendant sparking, burning, melting, and smoking.
Medline is recalling Full Electric Basic Homecare Beds because the hand control pendant may overheat and catch fire in rare scenarios. The company has received 58 complaints of pendant sparking, burning, melting, or fire.
Medline recalls IV administration kits because check valve components may become stuck, potentially affecting medication delivery. The recall affects 5,314 units distributed nationwide.
Medline is recalling robotics urology procedure kits with Stryker Strykeflow 2 Suction Irrigators due to a 2024 design change that allows irrigation solution to leak and emit vaporized saline during use.
Medline kits containing B. Braun IV Administration Sets are recalled because check valve components may become stuck, potentially affecting medication delivery. Lot Number 25HBQ850 is affected.
Medline medical procedure kits containing Stryker Strykeflow 2 suction irrigators are being recalled due to a 2024 design change. Irrigation solution can travel to the handpiece and battery pack, causing leaks and vaporized saline emission resembling smoke.
Medline Industries recalls pre-operative kits containing B. Braun IV administration sets because their check valve components may become stuck in open or closed positions, potentially affecting fluid delivery.
Medline medical procedure kits containing Stryker Strykeflow 2 suction irrigators are recalled. A 2024 design change causes irrigation solution to leak and vaporized saline to emit during use.
Medline has recalled approximately 1,725 IV Administration Sets containing B. Braun components because check valves may become stuck in open or closed positions, potentially preventing medication delivery or allowing uncontrolled fluid flow.
Medline is recalling IV administration kits containing B. Braun components because check valves may become stuck in the open or closed positions. The recall affects 338 units distributed nationwide.