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Medline Industries is recalling Medline Namic Control Syringes (Model DYNJSYR10CWRB) because the FDA has rescinded their 510(k) regulatory clearance. The recall affects 24,170 units distributed nationwide.
Medline Industries has recalled the GYN Laparoscopy Pack (Model DYNJ41257F, Lot 25GBL423) because its regulatory clearances for certain components—including Control Syringes, Guidewires, and High-Pressure Tubing—have been rescinded.
Medline Industries has recalled multiple control syringes, guidewires, and high-pressure tubing models because their FDA 510(k) regulatory clearances have been rescinded. The recall affects 38,230 units distributed nationwide.
Medline Industries is recalling certain surgical and medical kits because their 510(k) regulatory clearances for Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. About 2,609 units were distributed nationwide.
Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed nationwide and internationally.
Medline Industries is recalling certain Angio Cath Pack kits (Model DYNJ24517D, Lot 25CBA224) because their regulatory 510(k) clearances have been rescinded by the FDA.
The FDA has rescinded the 510(k) regulatory clearances for certain Control Syringes, Guidewires, and High-Pressure Tubing components in Medline's General Laparoscopy Kit (Model CDS930027Y). Affected units should not be used.
Medline Industries is recalling D and C Pack kits (Model DYNJ41254B) nationwide because regulatory clearances for certain Control Syringes, Guidewires, and High-Pressure Tubing have been rescinded.
The FDA has rescinded regulatory clearances for certain Control Syringes, Guidewires, and High-Pressure Tubing included in Medline's Arthroscopy Pack (Model DYNJ82440). Affected units should not be used.
Medline Industries is recalling 19,189 cardiac catheterization kits nationwide because certain syringe, guidewire, and tubing components had their FDA premarket notification (510(k)) clearances rescinded, meaning they were distributed without valid regulatory authorization.
Medline Industries has issued a recall of Medline Namic Guidewires because their FDA 510(k) regulatory clearances have been rescinded. The affected units were distributed nationwide.
Medline Industries is recalling Medline Convenience Kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance.
Medline Industries is recalling Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance.
Medline's CENTURION Circumcision Kits (Lot 25KLA002) were distributed non-sterile. Healthcare facilities and patients who received them should not use the affected kits.
Medline recalls 3,120 medical convenience kits containing control syringes due to a potential risk that the rotating adaptor could unwind during use, causing loose or complete disconnection from the manifold.
Medline Industries is recalling 1,698 medical convenience kits containing angiographic syringe adaptors that may unwind during use, causing loose or disconnected connections between components.
Medline Industries is recalling 594 medical convenience kits containing NAMIC syringe rotating adaptors that may unwind and disconnect during use. The kits were distributed worldwide.
Medline Industries is recalling 82 surgical convenience kits because the rotating adaptor on the included syringes may unwind during use, potentially causing the syringe to disconnect from the manifold.
Medline is recalling 439 medical convenience kits worldwide containing defective NAMIC Angiographic RA Control Syringes. The syringe rotating adaptor may unwind during use, causing loose or full disconnection between the syringe and manifold.
Medline Industries is recalling medical convenience kits containing NAMIC Angiographic Rotating Adapter (RA) Control Syringes due to a risk that the syringe adaptor may unwind during use, causing disconnection from the manifold. Worldwide distribution includes the US, Canada, and nine other countries.
Medline Industries is recalling medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes that may unwind during use, causing loose or complete disconnection between the syringe and manifold.
Medline is recalling medical convenience kits containing syringe adaptors that could loosen or disconnect during catheterization procedures.
Medline is recalling NAMIC Angiographic Syringes because the rotating adaptor may unwind during use, causing loose or full disconnection from the manifold. The FDA classified this as a Class I recall.
NAMIC Angiographic Syringes may have rotating adaptors that unwind during use, causing loose or complete disconnection from the manifold, affecting 2.6 million units distributed worldwide.
Medline is recalling angiographic syringes because the rotating adapter may unwind during use, causing loose or complete disconnection between the syringe and manifold.