Every recall we track for Medline Industries, LP — 505 in all — plus the complaints and injury reports the public filed about them.
Medline recalls specific neonatal breathing circuits due to potential overheating that could cause infant breathing problems. Affected models include HUD78001KIT to HUD88017KIT kits. Stop using immediately if you own these products.
Medline recalls Hudson RCI heated breathing circuits (SKU HUD78019) due to potential infant respiratory failure from sporadic heating failures. Affected units may show discoloration, melting, or burning smells. Stop using immediately to prevent serious breathing issues.
Medline recalls neonatal breathing circuits with potential sporadic failure causing infant respiratory issues. Discard or return affected units to avoid risks of airway obstruction and breathing complications.
Medline recalls specific surgical convenience kits with potentially contaminated components. Affected kits include LAVH, GYN ABDOMINAL CDS, and other surgical kits with listed SKUs and lot numbers. Consumers should check their kits against the provided details.
Medline recalls convenience kits labeled MAJOR HEAD AND NECK PPS with SKU DYNJ9425991S due to potential contamination. Affected kits have specific UDI/DI and lot numbers.
Medline recalls 10 different convenience kits with potentially contaminated components. Consumers should check product labels for specific SKUs and lot numbers to determine if their kit is affected.
Medline recalls 16 different GYN robotic surgical kits with potentially contaminated components. Consumers should stop using these kits immediately to avoid health risks.
Medline recalls two convenience kits (FEMORAL PACK SKU DYNJ909393A and FEVAR SKU DYNJ910295D) due to potentially contaminated components. Affected kits have specific lot numbers and were sold in 2023-2024.
Medline recalls medical convenience kit TRACH TUBE KIT (SKU DYKM2330) due to labeling discrepancy. Affected units have specific UDI/DI and lot numbers. No remedy stated in official notice.
Medline recalls 14 surgical convenience kits due to potentially contaminated components. Affected kits include GYN Lithotomy, Major GYN Pack, and others with specific SKUs and lot numbers. Consumers should check their kits for listed identifiers.
Medline recalls convenience kits labeled LTP CDS-LF and SKU CDS98037: potentially contaminated components. Consumers should check product details and contact Medline for guidance.
Medline recalls specific C-Section convenience kits due to potentially contaminated components. Affected kits include SKUs DYNJ904612L, DYNJ911755, and DYNJ912014 with certain lot numbers. Consumers should check their kits for these identifiers.
Medline recalls several surgical convenience kits with potentially contaminated components. Affected kits include specific SKUs and lot numbers for major procedure and laparoscopy kits.
Medline recalls convenience kits with potentially contaminated components. Affected kits include CMH LITHO MINOR PACK-LF, EAST MAJOR LITHOTOMY, GYN LAPAROTOMY, and UNIVERSAL GYN models. Consumers should check their kit's SKU and lot number for recall.
Medline recalls several convenience kits with potentially contaminated components. Consumers should check product labels for specific SKUs and lot numbers to determine if their kit is affected.
Medline recalls specific medical convenience kits due to potential out-of-specification endotoxin levels in Neurosponges. Affected kits include LAMINECTOMY PACK and ORTHO SPINE PACK models with listed SKUs and lot numbers.
Medline recalls specific medical convenience kits with neurosponges that may have unsafe endotoxin levels. Affected kits include CRANIOTOMY PACK and ORTHO SPINE PACK models. Consumers should check their kits for listed SKUs and lots to avoid potential health risks.
Medline recalls specific neurosponge kits due to possible endotoxin levels exceeding specifications. Affected kits include NEURO CDS, NEURO PACK, and other medical convenience kits with listed SKUs and lot numbers.
Medline recalls specific medical convenience kits due to potential endotoxin levels in Neurosponges. Affected kits include SINUS PACK-LF and ENT PACK models with certain SKUs and lot numbers.
Medline recalls 150-count germicidal bleach wipes that may have reduced bleach concentration, risking less effective disinfection. Affected items were sold from May 2025 to May 2026.
Medline recalls 150-count germicidal bleach wipes that may have reduced bleach concentration, risking less effective disinfection. Affected items sold between May 2025 and April 2026.
Medline recalls 110-count bleach wipes due to potential reduced bleach concentration before 12-month shelf life, risking less effective disinfection.
Medline recalls Micro-Kill Bleach Germicidal Wipes due to potential reduced bleach concentration before 12-month shelf life, risking less effective disinfection. Affected products include 110-count bags with specific product numbers and production dates.
Medline recalls specific Neuro Pack medical kits that may contain low levels of Bacillus species. Affected kits have SKUs DYNJ59397P and lot numbers listed. Contamination could pose health risks.
Medline recalls specific pediatric heart Moses kits with BD PurPrep 26mL that may have low levels of Bacillus species. Affected kits include models DYNJ910103B and DYNJ910961A with certain lot numbers.
Medline recalls specific medical convenience kits that may contain low levels of Bacillus species. Affected kits include TOTAL JOINT PACK and EXTREMITY/FOOT PACK models with certain lot numbers. Consumers should check their kit's SKU and lot number to determine if recalled.
Medline recalls specific medical convenience kits containing BD PurPrep 26mL that may be contaminated with low levels of Bacillus species. Affected kits include Shoulder Pack and Major Ortho Kit models with certain lot numbers.
Medline recalls knee surgery kits with Zimmer Biomet mixing bowls and spatulas that may cause sterility breaches, leading to extended surgery time to find alternative devices.
Medline recalls knee surgery kits with Zimmer Biomet mixing bowls and spatulas that may cause sterility breaches, requiring replacement to prevent infection risks during surgery.
Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific UDI codes and lot numbers.
Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) due to surface material that may cause staining and potential harm. Affected kits have specific lot numbers and were sold with certain medical procedures.
Medline recalls HIP CDS-LF medical procedure kits with specific SKUs due to quality issues that may cause pain management drugs to be ineffective.
Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16-20) due to increased surface raw material causing potential staining and harm. Affected kits have specific lot numbers and UDI codes.
Medline recalls convenience kits containing Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface material that may cause staining and potential harm. Affected kits include specific model numbers and lots.
Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific model numbers and lot codes.
Medline recalls convenience kits containing Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific lot numbers and were sold by Medline.
Medline recalls convenience kits containing Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface material that may cause staining and potential harm.
Medline recalls convenience kits containing Bard Silastic Foley Catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific lot numbers and UDI codes.
Medline recalls convenience kits with Bard Silastic Foley catheters (French sizes 16, 18, 20) due to increased surface raw material causing potential staining and harm. Affected kits have specific lot numbers and UDI codes.
Medline recalls specific knee and hip procedure kits due to quality issues with pain management drugs that may not work as intended.
Medline recalls specific convenience kits containing Bupivacaine Hydrochloride in Dextrose Injection due to quality issues from Huons Co, Ltd. Affected kits have unique SKUs and lot numbers listed in the recall notice.
Medline recalls specific C-SECTION kits containing Bupivacaine Hydrochloride due to quality issues from Huons Co, Ltd. Affected kits have unique SKUs and lot numbers.
Medline recalls specific anterior hip kits containing Bupivacaine Hydrochloride in Dextrose Injection due to quality issues from the supplier. Affected kits have unique identifiers and lot numbers.
Medline recalls two convenience kits with temperature probes that may have been distributed incorrectly. Affected kits include specific model numbers and lot numbers. Consumers should check their kits and contact Medline for details.
Medline recalls specific convenience kits with temperature probes due to a distribution error. Affected kits include models DYNJ88569 and variants with certain lot numbers. No immediate action is required but check your kit for the listed model numbers and lot codes.
Medline recalls convenience kits containing Swan-Ganz catheters (DYNJ905503D/F/G) due to risks of leaks, breakage, and potential infection from faulty blue proximal hubs.
Medline recalls convenience kits containing Swan-Ganz catheters (model DYNJ68530B) due to risks of leaks, breakage, and infection. Affected kits have specific lot numbers.
Medline recalls convenience kits containing Swan-Ganz catheters CDS982269K-L and DYNJ901328D-F models that may leak or break, causing infection or blood loss. Affected kits were sold with specific lot numbers.
Medline recalls convenience kits containing Swan-Ganz catheters (model DYNJ68530A) due to risks of leaks, breakage, and infection. Affected kits have specific lot numbers.
Medline recalls specific convenience kits containing temperature probes with a distribution error. Affected kits may have safety risks; contact Medline for details.
Medline recalls convenience kits with Swan-Ganz catheters (DYNJ8407) due to potential leaks and breakage from catheter hub failures, risking infection and blood loss.
Medline recalls convenience kits with Swan-Ganz catheters that may leak or break, risking infection and blood loss. Affected kits have specific model numbers and lot codes.
Medline recalls convenience kits with Swan-Ganz catheters linked to leaks and breakage, risking infection and blood loss. Affected kits include specific model numbers and lots.
Medline recalls convenience kits with Swan-Ganz catheters that may leak or break, risking infection or blood loss. Affected kits include Germantown and University CABG models.
Medline recalls L&D Continuous Epidural Trays (PAIN1699A) due to FDA-identified quality issues in Lidocaine Ampules. Affected units include specific model and lot numbers.
Medline recalls 34 convenience kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules due to quality issues found during FDA inspection.
Medline recalls convenience kits with Huons Lidocaine Ampules due to FDA manufacturing quality issues. Affected kits include specific models and lot numbers. Consumers should contact Medline for details.
Medline recalls two convenience kits due to quality issues with Lidocaine Ampules identified during FDA inspection. Affected kits include ART890B and IVS3350 models with specific lot numbers. Consumers should contact Medline for details.
Medline recalls convenience kits containing Lidocaine injections due to FDA-identified quality issues at the manufacturer's facility. Affected kits have specific model numbers and lot codes.
Medline recalls Convenience Kits Block Tray Model DYNJRA1590 due to quality issues found during FDA inspection of Huons Co. Ltd.'s manufacturing site. Affected units contain Lidocaine Ampules with potential safety risks.
