Medline

Medline has recalled certain medical convenience kits (SKU # DYNJ80513B) because the syringe rotating adaptor can unwind during use. This may cause the syringe to become loose or fully disconnect from the manifold, potentially affecting medical procedures.

Medline has recalled medical convenience kits containing NAMIC Angiographic Rotating Adaptor (RA) syringes because the syringe connector may unwind during use. This can cause a loose or complete disconnection between the syringe and the manifold, potentially interrupting medical procedures.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline Industries has recalled multiple batches of NAMIC Angiographic Syringes because the rotating adaptor that connects the syringe to medical tubing may unwind during use. This can cause the syringe to loosen or disconnect completely from the manifold, potentially disrupting fluid delivery during medical procedures.

Medline medical convenience kits containing NAMIC angiographic syringes may have a rotating adapter that can unwind during use. This could cause the syringe to loosen or fully disconnect from the manifold during cardiac catheterization procedures. No injuries have been reported, but the disconnection poses a risk during medical use.

Medline Industries is recalling five medical convenience kits that contain syringes with rotating adapters that may unwind during use. This could cause the syringe to loosen or fully disconnect from the manifold. No injuries have been reported.

Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.

Medline's NAMIC Angiographic Control Syringes may have a rotating adapter that can unwind during use, causing the syringe to disconnect from the manifold. This could interrupt fluid delivery during medical procedures. The issue was found through post-market monitoring.

Medline Industries has recalled multiple models of NAMIC angiographic syringes because the rotating adaptor connecting the syringe to the manifold may unwind during use. This could cause the syringe to disconnect or loosen, potentially interrupting a medical procedure.

Medline's Anterior Hip Pack surgical kits contain Olympus biopsy valves that may shed rubber fragments. These fragments could lodge in a patient's airway during a procedure, potentially requiring removal and causing breathing problems or inflammation.

Kits contain recalled Olympus biopsy valves. Olympus is investigating an increase in complaints associated with rubber fragment detachment in the slit of single use biopsy valves. Potential consequences associated with detachment of fragments from valve include foreign body in patient's tracheobronchial tree, which may require intervention for removal. Other potential consequences include inflammatory response, hypoxia, and prolongation of procedure.

Medline kits containing Olympus biopsy valves may have rubber fragments that can detach inside the valve. These fragments could lodge in a patient's airways during a procedure, potentially requiring removal and causing inflammation or reduced oxygen levels.

Medline kits containing Olympus biopsy valves may have rubber fragments that can detach inside the valve. These fragments could enter a patient's airway and require removal, or cause inflammation and breathing problems. Olympus is investigating complaints about this issue.

Medline's thoracic robot kits contain Olympus biopsy valves that may shed rubber fragments during use. These fragments could lodge in a patient's airway, potentially requiring removal and causing breathing problems or inflammation.

Medline convenience kits containing Olympus biopsy valves may have defective valves that shed rubber fragments during use. These fragments could lodge in a patient's airway, potentially requiring removal and causing inflammation or breathing problems.

Medline's Airway Exam Kit contains Olympus biopsy valves that may shed rubber fragments. These fragments can lodge in a patient's airway and may require removal. This could cause inflammation, low oxygen levels, or extend the procedure time.

Medline Industries identified a potential breach in the sterile pouch packaging of one lot of Sterile Radiology Procedure Kits (Model DYNDH1491B). This breach may allow the kit to lose its sterile condition. No injuries have been reported.

Medline Industries recalled two G-tube care kits (SKU DYKM2720 and SKU ENFITDISCKIT) because the connectors were not made to the right size. This means they may not seal properly with ENFit-style feeding tubes, which could cause leakage of nutrition or fluids. If you try to tighten the connector to stop leaking, it could cause injury, infection, or discomfort.

Medline's ENFIT G-tube connectors (Item No. ENFIT1010GC) were not made to the correct specifications and may not seal properly with ENFit-style medical devices. This can cause leakage of feeding fluids and delay necessary care. If users tighten the connector too much to stop the leak, it can cause infection, discomfort, and require additional medical treatment.

Medline Industries has recalled specific lots of Puracol and Puracol Plus collagen wound dressings due to elevated endotoxin levels. These contaminants can cause inflammation, tissue irritation, delayed healing, fever, low blood pressure, and in severe cases, septic shock.

Medline surgical drapes and gowns may fall apart (delaminate) when washed using the included instructions. If a delaminated drape is used during surgery, it could tear and allow bacteria through, increasing infection risk.

Medline surgical gowns may develop fabric separation (delamination) when laundered using the included instructions. If a separated gown is used during surgery, fluid or bacteria could pass through the compromised fabric, potentially increasing infection risk.

Medline and Cardinal Health have recalled specific lots of chest drainage kits used in cardiac surgery because the instructions needed to clarify that these devices are intended only for adult patients age 18 and older. The kits were distributed nationwide in California and internationally to Chile and Panama.

Medline dialysis dressing change convenience kits (SKU DYNDC3167) may contain defective Tego Connectors with silicone seal problems. The seals can dome or tear, which may block fluid flow, cause therapy delays, leak fluids, or allow air or contamination into the bloodstream.

Medline Industries is recalling several dialysis and pheresis dressing change kits because the silicone seals on included Tego Connectors may be damaged, domed, or torn. A damaged seal can prevent blood withdrawal or injection, cause fluid leakage, delay treatment, or allow air or contaminants into the bloodstream.

Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.

Medline dialysis kits containing Tego Connectors may have defective silicone seals that can dome or tear. This can block the fluid path, prevent blood withdrawal, cause fluid leaks, interrupt treatment, or allow air and contaminants into the body.

Medline dialysis on/off kits may contain Tego Connectors with defective silicone seals that can dome or tear. This can block the fluid path, prevent blood product injection or withdrawal, cause fluid leakage, delay treatment, or allow air or contaminants into the body.

Medline Industries is recalling two dialysis insertion kits that contain Tego Connectors with defective silicone seals. The seals may dome or tear, which can block fluid flow, cause therapy delays, allow leaks, or introduce air or contamination into the body.

Meijer sterile saline wound wash (0.9% sodium chloride, 7.1 fl oz) may not have been manufactured to meet required sterility standards. The manufacturer did not follow proper sterilization procedures for this wound-cleaning product. All lots of model MJSALINE7 are affected.