283 recalls found for Medline Industries, LP. Check if any of your products are affected.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Medline Industries, LP recalled 149,439 NAMIC Angiographic Syringes worldwide, including the US and several international markets. The post-market signal shows a potential rotation adaptor unwinding during use, which can cause a loose or complete disconnect with the manifold. Health care providers and patients should stop using the devices and follow Medline's recall instructions.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline Industries, LP recalled 594 medical convenience kits worldwide, including NAMIC Angiographic Rotating Adaptor syringes, due to a potential unwinding of the syringe adaptor that can cause a loose connection or disconnection with the manifold.
Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.
Unapproved design changes to the products outside of the 510(k) clearance.
Unapproved design changes to the products outside of the 510(k) clearance.
Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.
Medline Industries, LP recalls 2,154 medical convenience kits worldwide after post-market surveillance found a risk that the NAMIC Angiographic Rotating Adaptor may unwind. A loose connection or disconnection between the syringe and manifold could occur. Stop using immediately and follow manufacturer recall instructions.
Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed
Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.