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Medline Industries, LP alerts
Verified recalls, refunds, lawsuits, and settlements involving Medline Industries, LP.
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain a potentially contaminated component which were recalled by the manufacturer Product details: Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of the labeled 12-month shelf life. Reduced...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The procedure kits contain ICU Medical, Inc. pain management kits containing Bupivacaine Hydrochloride in Dextrose Injection, USP, which were recalled due to quality issues that could...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Affected kits contain recalled Bard Silastic Foley Catheters. Catheters were recalled by manufacturer due to increased amount of raw material present on the surface of the catheter. Issue...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline Industries, LP is issuing a recall for specific Medline convenience kits containing BD PurPrep 26 mL which may be contaminated with low levels of Bacillus species. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for Lidocaine Ampules due to quality...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Firm identified unapproved design changes to the products outside of the 510(k) cleared by the FDA. Products not initially reported in RES 98601. Product details: Convenience kits...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application. Product details:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality issues, including microbiology testing...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Specific Medline Kits contain Cardinal Health Monoject 1mL Luer Lock Syringes, Tuberculin Print, Sterile. Cardinal Health has recalled these syringes because the outer carton and blister...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified the presence of particulate within the fluid path of the Manifolds. Product details: Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified the presence of particulate within the fluid path of the Manifolds. Product details: Namic Preceptor Manifold, custom, Medline Product Number/SKU 64037107;...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
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...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
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...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
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...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
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...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
Unapproved design changes to the products outside of the 510(k) clearance. Product details: Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) CATH LAB CDS, Model Number:...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration
Recall
Active
FDA
Official source
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded. Product details: Medline Kits: 1) ANGIOGRAPHY PACK-LF, Model...
- Company
- Medline Industries, LP
- Deadline
- No deadline listed
- Source
- U.S. Food and Drug Administration