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 is recalling anesthesia convenience kits with cracked tubing that may leak, risking hypoxia, hypoventilation, and inadequate anesthetic delivery during surgery.
Medline Industries is recalling 96,406 anesthesia circuit kits due to cracks in expandable tubing that may cause leaks, leading to hypoxia, hypoventilation, and inadequate anesthetic delivery. These defects may result in serious injury or death.
Medline's anesthesia circuit kits for robotic surgical systems are recalled due to tubing cracks that can leak, potentially causing inadequate anesthesia delivery during surgery. Affected patients could experience hypoxia and hypoventilation.
Medline Industries is recalling certain Ligasure surgical devices that may trap residual material, which could dislodge during laparoscopic procedures. Approximately 60,917 units distributed nationwide are affected.
Medline Renewal is recalling certain LigaSure Blunt Tip Sealer/Divider devices with firmware 4.0.1.15 or lower because residual material may trap within the device and in rare cases become dislodged.
Medline Renewal is recalling LigaSure Impact Sealer/Divider surgical devices because certain areas can trap residual material that may rarely become dislodged during procedures.
Medline Industries is recalling 58,499 units of its Renewal Ligasure Impact Sealer/Divider nationwide due to potential entrapment of residual material that may become dislodged during use.
Medline is recalling certain RenewalLigasure Blunt Tip Sealer/Divider devices due to potential material retention in device areas that may rarely become dislodged during surgery. No injuries have been reported.
Medline Industries recalls the Renewal LigaSure Maryland Jaw Sealer/Divider because certain areas can trap residual surgical material that may dislodge during use.
Medline Industries is recalling the Medline Renewal LigaSure Exact Dissector due to areas on the device that may trap residual material. In rare cases, trapped material could become dislodged.
Medline is recalling 18,117 units of LigaSure Small Jaw surgical instruments because certain device areas can trap residual material inside. In rare cases, this material may become dislodged during use.
Medline Industries is recalling 1,446 Renewal Ligasure Sealer/Divider electrosurgical devices distributed nationwide. Residual surgical material may become trapped in certain areas and, in rare cases, become dislodged during use.
Medline Industries is recalling 9,547 Ligasure Maryland Jaw Sealer/Divider devices due to the potential to trap residual material. In rare cases, this material may become dislodged.
Medline Industries is recalling a surgical sealer device that may trap residual material internally, which could become dislodged in rare cases. The Class II recall affects 4,007 units distributed nationwide.
Medline Industries is recalling Excelsior Medical saline IV flush syringes because a limited quantity may not meet required sodium chloride concentration. Approximately 8.3 million units are affected.
Medline Industries is recalling 222,800 units of Alcohol Prep Pads nationwide due to subpotency. The pads may not contain the labeled 70% isopropyl alcohol concentration.
Medline Industries is recalling Adult Anesthesia Sets containing Clearlink IV Sets that Baxter recalled due to customer reports of leaking. Healthcare facilities should discontinue use of affected sets.
Medline is recalling reprocessed ACUSON AcuNav ultrasound catheters that may have residual particulates, creating risk of infection, blood clots, or embolism.
Medline Industries is recalling two sterile convenience kit models because the products were not sterilized despite being labeled as sterile. The kits were distributed to Florida, Maryland, New Jersey, and Tennessee.
Medline Industries recalled certain lots of reprocessed Webster CS Catheters due to residual particulates on patient-contacting surfaces that may cause infection, blood clots, or embolism.
Medline Industries recalls 88 Extremity Pack convenience kits that were labeled as sterile but did not undergo sterilization. The affected units were distributed to healthcare facilities in Florida, Maryland, New Jersey, and Tennessee.
Reprocessed electrophysiology catheters may contain residual particulates, potentially causing infection, inflammation, blood clots, or embolism. The FDA classified this Class I recall affecting 7,913 units.
Medline is recalling 828 units of VALVE PACK-LF catheter kits because the catheter may not retain its shape, potentially causing device malfunction.
Medline is recalling over 7,900 reprocessed electrophysiology catheters due to potential residual particulates on patient-contacting surfaces that could cause infection or blood clots.
Medline is recalling 7,913 reprocessed ICE catheters due to residual particulates on patient-contacting surfaces. These particles may cause infection, blood clots, or potentially fatal embolism.