Medical device recalls (page 16)
2545 recalls.
- Medline Convenience Kits: 1) NEURO SHUNT- CODMAN recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CHEST TUBE INSERTION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ADMIT KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PPE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CENTRAL LINE UNIVERSAL INSERTI recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) CVC PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) DRAWER 6-IV FLUIDS GLOVES recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) LITHOTOMY PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) MAJOR LAPAROTOMY CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for full list. Medline Convenience Kits: 1) CHP COCHLEAR SUPPLEMENT CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) DYNDA3003 recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) PICC LINE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - See RES for complete list. Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANGIO PROCEDURE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANGIO PROCEDURE PACK recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) SCC RF PAIN MGMT recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - Medline Convenience Kits: 1) ANCILLARY PACK-LF recall (Medline Industries, LP)
Medical deviceClass IIReported May 13, 2026 · Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated... - One Step P in vitro diagnostic test REF: 8194 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step K in vitro diagnostic test REF: 81A4 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - Uric Acid in vitro diagnostic test REF: 31H0P recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - QUCARE Total Cholesterol in vitro diagnostic test REF: 6407 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step pH in vitro diagnostic test REF: 31I4P recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step UTI in vitro diagnostic test REF: 3374 recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - One Step 10A in vitro diagnostic test recall (DFI Co., Ltd.)
Medical deviceClass IIReported May 13, 2026 · The devices were distributed without required FDA premarket clearance or approval. - Biofire Spotfire Respiratory/Sore Throat Panel REF: 423485 recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Respiratory/sore throat panel test may result in false negative results and control failures. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining... - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - DEX Ophthalmic Tissue Forceps recall (Katalyst Surgical, LLC)
Medical deviceClass IIReported May 13, 2026 · Field Safety Corrective Action for IFU in DEX Forceps and Scissors. - Mint Lesion recall (Mint Medical GmbH)
Medical deviceClass IIReported May 13, 2026 · If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be... - BioFire Joint Infection recall (BioFire Diagnostics, LLC)
Medical deviceClass IIReported May 13, 2026 · Contamination to in-vitro diagnostic test may result in false positives. - LIFEPAK 15 recall (Physio-Control, Inc.)
Medical deviceClass IIReported May 13, 2026 · Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was... - ERBEFLO 2 recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module ... recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester). - Prodisc C SK U.S. IMPLANT EXTRA LARGE 6MM. Model Number: PDSXL6. Total cervical... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc... recall (Centinel Spine, Inc.)
Medical deviceClass IIReported May 13, 2026 · Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was... - LUX-Dx II Plus recall (Boston Scientific Corporation)
Medical deviceClass IIReported May 13, 2026 · For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or... - LUX-DX II recall (Boston Scientific Corporation)
Medical deviceClass IIReported May 13, 2026 · For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or... - Brand Name: Da Vinci X and Da Vinci Xi Product Name: da Vinci X recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported May 13, 2026 · Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking. - Medical Action Industries Inc. Pack Cath BHH recall (Medical Action Industries, Inc. 306)
Medical deviceClass IReported May 13, 2026 · Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the... - Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating... recall (American Contract Systems Inc)
Medical deviceClass IReported May 13, 2026 · Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full... - Halyard VA DETROIT CATH LAB PACK kit. Model Numbers: VMCD029. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard SAMMC ANGIOGRAPHY kit. Model Numbers: SAMM066-15. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard PERC TRAY kit. Model Numbers: SLPC34-01 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard NEURO IR PERIPHERAL recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard HEART CATH recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75-01. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CATH LAB kit. Model Number: SACL75AM. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK SAN23CARDQ kit. Model Number: DRCC36. recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - Halyard CARDIAC CATH PACK kit. Model Number: EAMC1000-05 recall (AVID Medical, Inc.)
Medical deviceClass IReported May 13, 2026 · Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe... - VOCSN V+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported May 13, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions... - Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G31213 ... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G47308 ... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Catheters... recall (Cook Incorporated)
Medical deviceClass IReported May 13, 2026 · Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated... - Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06 recall (Intuitive Surgical, Inc.)
Medical deviceClass IReported May 13, 2026 · Reloads for curved-tipped stapler may potentially produce an incomplete staple line. - Medline and Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Medline or Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Medline and Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Medline medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Centurion medical convenience kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · 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... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Centurion medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline and Centurion medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market... - Medline medical procedure kits recall (Medline Industries, LP)
Medical deviceClass IIReported May 6, 2026 · During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market...