Every recall we track for Cardinal Health 200, LLC — 264 in all — plus the complaints and injury reports the public filed about them.
Cardinal Health recalls specific surgical kits due to unexpected endotoxin level variations in MEDICOM Ritmed Neurological Sponges, which could pose health risks during medical procedures.
Cardinal Health recalls 11 surgical kit types due to unexpected endotoxin variability in Medicom Ritmed Neurological Sponges, which could pose risks during procedures.
Cardinal Health recalls Presource Kits with NEWNAN SMR PACK (Catalog SEN21SPPMB) due to unexpected endotoxin variability in Neurological Sponges. Affected lots from 2019-2020 may pose risks.
Cardinal Health 200, LLC
Cardinal Health 200, LLC product list with detailed information including part numbers, lot numbers, and UDI-DI codes.
Cardinal Health 200, LLC
Cardinal Health recalls specific presource kits with neuro sponges that have unexpected endotoxin level variations. These kits may pose risks during medical procedures.
Cardinal Health 200, LLC
Cardinal Health 200 LLC recalls 200-count Webcol Alcohol Prep pads (70% isopropyl alcohol) due to microbial contamination with Paenibacillus phoenicis. Affected lots include specific batch numbers listed in the recall notice.
Cardinal Health recalls 1mL Luer Lock Tuberculin Syringes that contain U-100 insulin syringes instead of tuberculin syringes. This mismatch risks incorrect medical use.
Cardinal Health recalls chest drainage units for adults only; using on infants may cause treatment delays and prolonged hospitalization due to lack of tidaling/bubbling.
Cardinal Health recalls ChemoPlus gowns with incorrect expiration dates on packaging. Product has a 3-year shelf life but is mislabeled as 5 years. Affected items include specific product codes and lot numbers.
Cardinal Health recalls Salem Sump PVC tubes with anti-reflux valves due to reported breakage from excessive force. Consumers should check product codes and contact the company for guidance.
Cardinal Health recalls Salem Sump PVC tubes due to Anti-Reflux Valve breakage from excessive force. Affected models include 10FR-36IN to 18FR-48IN tubes with specific product codes. Consumers should check their units and follow safety guidance.
Cardinal Health recalls Salem Sump PVC tubes due to reported Anti-Reflux Valve breakage from excessive force during use. Consumers should check product codes and follow safety guidelines to prevent injury.
Cardinal Health recalls Salem Sump PVC gastroduodenal tubes due to reported Anti-Reflux Valve breakage from excessive force during use. Affected models include various sizes and lengths.
Cardinal Health recalls Salem Sump PVC stomach tubes due to reported Anti-Reflux Valve breakage from excessive force during use. Affected models include various sizes and lengths.
Cardinal Health recalls Salem Sump silicone stomach tubes with anti-reflux valve that may break under force, causing leaks. Consumers should check product codes and contact for guidance.
Cardinal Health recalls pediatric Kendall SCD Comfort Sleeves (SKU 84021P) due to software errors that could delay treatment. Affected units sold with SmartFlow controllers.
Cardinal Health recalls Kendall SCD Blended Comfort Sleeves (SKU 84021B) for potential software errors that may delay treatment. Affected units sold with SmartFlow controllers.
Cardinal Health recalls SCD Comfort Knee Length Small sleeves used with Kendall SCD Smartflow. Incorrect software may cause treatment delays due to system high pressure errors.
Cardinal Health recalls umbilical vessel catheters due to packaging defects that may compromise sterility, risking infection in neonates. Affected units include specific catalog numbers and lots.
Cardinal Health recalls umbilical vessel catheters due to packaging defect that may compromise sterility, risking infection in neonates. Affected units include specific catalog numbers and lots.
Cardinal Health recalls umbilical vessel catheters due to packaging defect that may compromise sterility, risking infection in neonates. Affected units include specific catalog numbers and lots.
Cardinal Health recalls umbilical vessel catheters due to packaging defects that may compromise sterility, risking infection in neonates. Affected units include specific catalog numbers and lots.
Cardinal Health recalls umbilical vessel catheters due to packaging defects that may compromise sterility, risking infection in neonates. Affected units include specific catalog numbers and lots.
Cardinal Health recalls umbilical vessel catheter insertion trays with packaging defect that may compromise sterility, risking neonatal infections. Affected units include specific catalog numbers and lots.
Cardinal Health recalls Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers.
Cardinal Health recalls 52 surgical kits due to potential endotoxin contamination in non-sterile strips and patties. Affected kits include specific catalog numbers and lot numbers for ophthalmology and ocular plastic packs.
Cardinal Health recalls two Presource Kit models due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected units include specific catalog numbers and lot numbers. Consumers should contact the manufacturer for details.
Cardinal Health recalls Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Consumers should contact Cardinal Health for details.
Cardinal Health is recalling Presource Kits with catalog numbers PE23NSMEA, PE23NSMEC, PE23SENLA, PE23SENLC, PE30EAGT6-9, PE30EAGTB, PE35NSB10-19, PE35NSBL1-19, PE3ESKSG1-2, PE3ESKSGA, PECGNAAU4-7, PEDHSPNH3, PEDHSPNHE, PEHDMJVCG, PEMHETMHA, PEMHNFMH1-2, PEMHNSB10-11, PEMHNSBH4-9, PEMHNSBHP, PEMHNSBHQ, PEMHNSBHR, PEV2CL011-106, PEV2FSNYA, PEV2FSNYB, PEV2OT10F, PEV2OT10G, PEV2OT10H, PEV2OT10I, PEX4SSMNA, PG35NSBL1, PG35NSBLA, PNVMESCH8, PNVMESCH9, PQMHETMHP due to potential endotoxin contamination in non-sterile surgical strips and patties. Consumers should stop using these kits immediately.
Cardinal Health recalls 70+ surgical kits with potential endotoxin contamination in non-sterile strips and patties. Affected kits have specific catalog numbers and lot numbers. Stop using immediately to avoid infection risks.
Cardinal Health recalls Presource Kits (major oral surgery and dental packs) due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected units include specific catalog numbers and lot numbers.
Cardinal Health recalls Presource Laryngoscopy Packs with potential endotoxin contamination in non-sterile surgical strips. Affected kits include specific catalog numbers and lot numbers. Consumers should contact Cardinal Health for details.
Cardinal Health recalls 330+ surgical kits for potential endotoxin contamination in non-sterile strips and patties. Affected kits include specific models and catalog numbers. Consumers should stop using recalled items immediately.
Cardinal Health recalls 35 Presource Kits for potential endotoxin contamination in non-sterile surgical strips and patties. Affected items include specific catalog numbers and lot numbers.
Cardinal Health recalls Presource Kits (catalog numbers PVV20110B, PVV20110D, PVV2CA103, etc.) due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits may pose infection risks during surgery.
Cardinal Health recalls robotic hysterectomy Presource Kits (PB4FRHWFA, PB4FRHWFB, PB4FRHWFC) due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits may pose infection risks during surgery.
Cardinal Health recalls 75+ Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Consumers should stop using affected kits to avoid infection risks.
Cardinal Health recalls Presource Kits (Laryngoscopy Pack) with catalog number SRIET0979N due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected units include specific lot numbers.
Cardinal Health recalls 62 surgical kits for potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include Ortho Plastic Microvascular PK and other spine/orthopedic kits with specific catalog numbers and lot numbers.
Cardinal Health recalls specific urology robotic packs due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include catalog numbers SOT4FRUWFA, SOT4FRUWFB, and SOT4FRUWFC with certain lot numbers.
Cardinal Health recalls 63 surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include CRANIOTOMY PACK and CHI STD NEURO CRANI OPT 4 models with specific catalog numbers and lot numbers. Consumers should stop using these kits immediately.
Cardinal Health recalls fetal surgery kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Consumers should contact Cardinal Health for details.
Cardinal Health recalls Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers listed in the recall notice.
Cardinal Health recalls Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Consumers should check their kits for these identifiers.
Cardinal Health recalls 328 Presource Kits with potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Consumers should check their kits for listed catalog numbers and lot numbers to determine if affected.
Cardinal Health recalls 329 Presource Kits for potential endotoxin contamination in non-sterile surgical strips and patties. Affected kits include specific catalog numbers and lot numbers. Stop using immediately to avoid infection risks.
Cardinal Health recalls AAMI Level 3 isolation gowns with product codes AT6100, AT6100-XL, AT6200, and AT6200-XL due to potential hydrostatic pressure failure. These gowns may not meet required protection standards.
Cardinal Health recalls Level 3 isolation gowns that may fail hydrostatic pressure tests, risking inadequate protection during medical procedures.
Cardinal Health recalls certain Monoject U-100 insulin syringes that may not work with needleless IV connectors. Stop using these syringes for IV push insulin to avoid potential incompatibility issues.
Cardinal Health recalls 4 models of Salem Sump Dual Lumen Stomach Tubes due to reported Anti-Reflux Valve breakage from improper use. No immediate action needed but label changes were made.
Cardinal Health recalls stomach tubes with anti-reflux valves that may break due to improper use. Affected models include 12-18 French sizes. No immediate action needed as labeling changes address the issue.
Cardinal Health recalls Presource kits and trays with specific catalog numbers due to potential patient harm from defective syringes. The syringes may cause inaccurate dosing or leaking.
Cardinal Health recalls specific Presource cardiac catheterization kits due to potential inaccurate dosing and leaking devices from syringes made by a Chinese manufacturer.
Cardinal Health recalls 23 neurological tray models with catalog numbers SAN29NICCA to SNEMHNTWDA due to potential inaccurate dosing and leaking devices from syringes made by Jiangsu Shenli Medical.
Cardinal Health recalls specific Presource kits and trays due to potential inaccurate dosing and leaking device risks from Shenli syringes. Affected kits include Cardiovascular Procedure Kits with catalog numbers SAN29ANCC3 through SAN73LHKC6.
Cardinal Health recalls X-Large adhesive bandages due to potential latex residue contamination. Affected models include 44102, sterile hypoallergenic bandages sold in 2019. No remedy specified in recall notice.
Cardinal Health recalls specific Jackson-Pratt 3-Spring Reservoir kits shipped without sterilization. Affected units have lot numbers starting with 210751D3. Consumers should stop using these kits to prevent infection risks.
