Medline Industries, LP recalls
Every recall we track for Medline Industries, LP — 576 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them. 34 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Medline Industries, LP peaked in 2025 (126); 576 since 2017. 6% rated “stop using now”.
All FDA recall records for Medline Industries, LP since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 16 | 63 | 45 | 2 | 126 |
| 2026 (to date) | 18 | 68 | 264 | 100 | 450 |
Most common reasons for Medline Industries, LP recalls
What to do if you have a recalled Medline Industries, LP product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Medline Industries, LP recalls
60 shown- Lower riskMedical device
Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
Medline recalls 30 Foot Ankle Convenience Kits (SKU DYNJ65395A) due to shelf-life discrepancy in a component. Affected kits have UDI/DI 10195327174156 (each) or 40195327174157 (case) and Lot 22GBW912. Return to Medline for replacement.
MedlineSep 11, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline surgical convenience kits labeled as: 1) OPEN HEART PACK A & B, Medline Product number/SKU DYNJ04584L; 2)
Medline Industries, LP is recalling DYNJ series medical devices due to potential safety issues. The recall affects products distributed nationwide in the US.
MedlineSep 2, 2026 - Use cautionMedical device
Medline Industries, LP recalls Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M
Medline recalls 3,551 convenience kits containing AirSeal Access Ports due to potential for erroneous overpressure alerts and system venting during surgery, which may delay or end procedures.
MedlineAug 31, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Rollator, Bariatric, Basic Steel, Blue, mechanical walker with four legs and a metal frame intended for medical
Medline recalls 835 bariatric rollators due to front wheel detachment risk. Check lot numbers and stop use immediately if affected.
MedlineAug 14, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Medline recalls 771,127 Basic Homecare Beds due to fire risk from hand control pendant overheating. Affected beds may smoke, spark, melt or catch fire. Stop using immediately.
MedlineAug 14, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
Medline recalls specific anesthesia L&D kits due to potential fungal contamination from Aspergillus penicillioides, which can cause serious infections or death. Affected kits have catalog numbers DYKMBNDL199A and specific lot numbers.
MedlineAug 11, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog
Medline recalls 109 convenience kits for potential elevated endotoxin levels in neurological sponges, which could cause medical issues like fever, inflammation, or low blood pressure. Affected kits have specific catalog numbers and lot numbers.
MedlineAug 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack
Medline recalls specific sinus packs containing Healthmark Instrument Channel Brushes with potential sharp edges that could cause cuts or infection. Affected units include SINUS PACK DYNJ48258D and DYNJ48258F models.
MedlineAug 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
Medline recalls anesthesia pain kits with potential open seals in sterile pouches that could cause patient infections if used without proper sterility checks.
MedlineJul 31, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Convenience Kit: OPEN HEART A PACK, Product Number DYNJ43008N
Medline recalls convenience kits with potential sterile barrier breaches causing infection risks. Affected kits may cause infections or complications if used after seal compromise.
MedlineJul 23, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A
Medline recalls convenience kits containing BD ChloraPrep Clear 1mL applicators from specific lots due to potential open seals causing infections. Affected kits may lead to skin or systemic infections if used.
MedlineJul 20, 2026 - Stop using nowMedical device
Medline Industries, LP recalls Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU
Medline recalls neonatal breathing circuits with potential sporadic failure causing infant respiratory issues. Affected models include HUD78007, HUD78009, and others. Stop using immediately if you have these circuits.
MedlineJul 13, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
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.
MedlineJul 10, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK,
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.
MedlineJul 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kits, labeled as: 1) NEURO CDS, Medline Kit SKU CDS985246J; 2) NEURO PACK, Medline Kit SKU
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.
MedlineJul 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Micro-Kill Bleach Germicidal Bleach Wipes, 6" x 5", 150 count, Product Number MSC351410AN
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.
MedlineJun 30, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
Medline recalls two types of convenience kits due to potential sterility breaches in packaging. If the sterile barrier is compromised, users may face infection risks. Affected kits have specific model numbers and lot numbers.
MedlineJun 12, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kits labeled as: 1) KIT PEDIATRIC OPEN HEART MOSES, Medline Kit SKU DYNJ910103B; 2) BASIC
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.
MedlineJun 11, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
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.
MedlineJun 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline convenience kits containing Bard¿ Silastic¿ Foley Catheters (French sizes 16, 18, 20) 5cc balloons. KIT
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.
MedlineJun 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls MEDLINE medical procedure convenience kit labeled as: 1) TOTAL KNEE-LF, Medline kit SKU CDSOPT590T; 2) TOTAL KNEE-LF,
Medline recalls specific knee and hip procedure kits due to quality issues with pain management drugs that may not work as intended.
MedlineJun 8, 2026 - UnratedMedical device
Medline Industries, LP recalls MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit SKU DYKS1574A; 2) TOTAL KNEE BASIC, Medline Kit
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.
MedlineJun 5, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Medline recalls specific convenience kits containing temperature probes with a distribution error. Affected kits may have safety risks; contact Medline for details.
MedlineMay 28, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG
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.
MedlineMay 28, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) SUTURE TRAY, Model Number: SUT12260; 2) CHEST TUBE INSERTION TRAY, Model Number: MNS3390;
Medline recalls 31 convenience kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules due to quality issues found during FDA inspection.
MedlineMay 21, 2026 - Use cautionMedical device
Medline Industries, LP recalls Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response"
Medline recalls reprocessed electrophysiology and ultrasound catheters with potential residual particles that could cause infection or blood clots if used. Affected lots include specific item numbers and dates.
MedlineMay 15, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV
Medline recalls two anesthesia kit models due to quality issues found during FDA supplier inspection. Affected kits contain lidocaine and bupivacaine injections. Consumers should check model numbers and lot numbers for affected items.
MedlineMay 6, 2026 - Lower riskMedical device
Medline Industries, LP recalls MEDLINE Medical Procedure Kits labeled as: 1) BASIC HEART PACK, Medline Kit/SKU DYNJ67331B; 2) CARDIAC SURGERY, Medline
Medline recalls 14 medical procedure kits with irregular catheter surfaces and connector detachment risks. Affected kits include BASIC HEART PACK and CARDIAC SURGERY models with specific SKUs and lot numbers.
MedlineMay 4, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline convenience kits: CMH CENTRAL LINE DRESSING CHANGE KIT EBSI1705A CVC/PICC/MIDLINE DRESSING CHANGE KIT EBSI1057A
Medline recalls specific convenience kits due to risk of butyrate tubing cracking, making products unusable for central line dressing changes.
MedlineApr 27, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
Medline recalls medical convenience kits labeled EYE TRAY-LF (SKU DYNJ21627P) due to incorrect syringes inside. The kits contain U-100 insulin syringes instead of the labeled 1mL Luer Lock Tuberculin syringes.
MedlineApr 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) BLOCK TRAY, Medline Kit
Medline recalls two kits containing Huons Bupivacaine HCL in Dextrose Injection due to microbiology testing concerns and reported efficacy complaints. Affected kits have specific SKUs and lot numbers.
MedlineApr 10, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: HEART CATH PACK-LF, Medline Kit Number/SKU
Medline recalls medical convenience kits with Namic Manifold (HEART CATH PACK-LF) due to particulate in fluid path. Affected kits have specific SKUs and lot numbers. Stop using immediately.
MedlineMar 24, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X
Medline recalls neuro sponges with higher-than-expected endotoxin levels that may be out-of-specification. Affected products include specific sizes and SKUs sold from 2019-2020.
MedlineMar 19, 2026 - Lower riskMedical device
Medline Industries, LP recalls CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Medline recalls Centurion Circumcision Kit (SKU CIT7050F) due to potential lack of sterilization, risking infection. Affected units sold with specific lot numbers.
MedlineMar 16, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: 1. BLOOD CULTURE KIT, Medline
Medline recalls blood culture kits with non-sterile Webcol alcohol prep pads due to contamination. Contaminated pads may cause infections during medical procedures. Affected kits have specific SKUs and lot numbers.
MedlineMar 16, 2026 - UnratedMedical device
Medline Industries, LP recalls Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR
Medline recalls convenience kits with select 10mL polycarbonate colored syringes that have unapproved design changes not cleared by the FDA. Products were not initially reported in RES 98601.
MedlineFeb 27, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA
Medline recalls medical convenience kits with NAMIC Angiographic Rotating Adaptor syringes that may unwind, causing loose connections or full disconnection. Affected kits include specific SKUs and lot numbers.
MedlineFeb 27, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes GU DAVINCI PACK - LF DYNJ909398A
Medline recalls convenience kits containing unapproved 10mL polycarbonate syringes with design changes not cleared by FDA. Affected kits have specific model numbers and lots. Consumers should check their kits for listed serial numbers.
MedlineFeb 27, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Kits: 1) HEART TRANSPLANT BIOPSY, Model Number: DYNJ37543A
Medline Industries recalls heart transplant biopsy kits with model DYNJ37543A due to rescinded 510(k) regulatory clearances. Affected kits may pose safety risks requiring immediate action.
MedlineFeb 25, 2026 - Lower riskMedical device
Medline Industries, LP recalls Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Medline recalls sterile radiology procedure kits with potential packaging breach that could compromise sterility. Affected kits have model DYNDH1491B and lot 25GBB924.
MedlineFeb 18, 2026 - Use cautionMedical device
Medline Industries, LP recalls THORACIC ROBOTS, DYNJ908777B
Medline recalls Thoracic Robots DYNJ908777B due to potential rubber fragments detaching from biopsy valves, risking airway obstruction and medical intervention.
MedlineFeb 16, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Medline recalls two kits with ENFIT G-Tube connectors that may leak due to improper sealing, risking fluid loss and infection. Affected kits have specific SKUs and UDI codes.
MedlineFeb 13, 2026 - Use cautionMedical device
Medline Industries, LP recalls Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP
Medline recalls Puracol and Puracol Plus collagen wound dressings with elevated endotoxin levels that may cause inflammation, delayed healing, fever, or septic shock if used.
MedlineFeb 10, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2)
Medline recalls specific Aqua-Seal Chest Drainage Units (models DYNJ902487A, DYNJ908126, DYNJ910851) for adults 18+ due to updated instructions clarifying target patient age.
MedlineJan 30, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL
Medline recalls surgical gowns with premature fabric delamination that may cause brief patient care delays or infection risk during surgery. Learn affected models and safety steps.
MedlineJan 28, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Kits containing Tego Connectors Medline DIALYSIS ON/OFF KIT SKU EBSI1746
Medline recalls dialysis kits with Tego Connectors due to silicone seal problems that could cause blood leaks or therapy interruptions. Affected kits include specific SKUs and production dates.
MedlineJan 8, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) KIT SURG ONC EXCISION BREAST, Model Number: DYKMBNDL84A; 2) KIT SURG ONC EXPLORATORY LAP,
Medline recalls 35 convenience kits for potential sterility issues due to calibration problems in sterilization packaging. Affected kits include specific models and lot numbers. Consumers should check their kits and contact Medline for details.
MedlineJan 7, 2026 - Lower riskMedical device
Medline Industries, LP recalls See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2)
Medline Industries, LP offers a wide range of medical products including supplies, equipment, and apparel. Explore our catalog for quality healthcare solutions.
Medline Industries, LPJan 7, 2026 - Lower riskMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) NAIL KIT, Model Number: DYKM1528
Medline recalls 15+ models of Nail Kits (DYKM1528) due to potential failure in sterility assurance for sterile saline wound wash. Consumers should check lot numbers on packaging.
MedlineJan 5, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number:
Medline recalls 23 IV administration sets that may leak, crack, or break during use, potentially causing blood loss, infection, or medication underdose. Affected models include DBD-IV ADMIN SET, 60DRP, and others with specific model numbers.
MedlineDec 31, 2025 - Stop using nowMedical device
Medline Industries, LP recalls Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit
Medline recalls 14 Fr Suction Catheter Kits (SKU DYND409:48625040001) due to possible inclusion of smaller 8 Fr catheters causing airway obstruction and respiratory failure.
MedlineDec 24, 2025 - Use cautionMedical device
Medline Industries, LP recalls Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE
Medline recalls specific medical kits with BD ChloraPrep Triple Swabsticks that may have open packaging seals. Affected kits include POWERGLIDE DRESSING CHANGE KIT SKU DYNDH1576 and CENTRAL LINE TRAY W/ CHLRP SWB SKU RWM-DC57KC. Stop using if you have these kits.
MedlineDec 24, 2025 - Stop using nowMedical device
Medline Industries, LP recalls Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec.
Medline recalls reprocessed Abbott Inquiry Steerable Diagnostic Catheters due to potential small particles causing inflammation, infection, or blood clots. Affected units include specific model numbers and lots.
MedlineDec 22, 2025 - Use cautionMedical device
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY PROSTATE, REF DYKMBNDL116G
Medline recalls specific medical procedure kits with Strykeflow 2 suction irrigators that may leak saline vapor during use, posing a risk of confusion with smoke. Affected kits have unique labels and lot numbers.
MedlineDec 16, 2025 - Lower riskMedical device
Medline Industries, LP recalls Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE
Medline recalls 28 medical procedure kits with MASTISOL liquid adhesive that cracks during vial actuation, potentially causing leaks. Check your kit's SKU and lot number for affected models.
MedlineDec 12, 2025 - Use cautionMedical device
Medline Industries, LP recalls MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L
Medline recalls lightweight homecare beds with hand control pendants that may overheat and cause fire if used beyond weight limits or with obstructions.
MedlineNov 26, 2025 - Use cautionMedical device
Medline Industries, LP recalls Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: DR HOLCOMB FACIAL
Medline recalls kits with B. Braun IV Administration Sets and Pump Administration Sets labeled DR HOLCOMB FACIAL due to check valve components potentially getting stuck, which could affect safe use.
MedlineNov 26, 2025 - Use cautionMedical device
Medline Industries, LP recalls Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED
Medline recalls Hudson RCI Medium Concentration Oxygen Masks due to tubing disconnecting during use, potentially causing shortness of breath and hypoxia. Affected models include 1041CE, HUD1035, HUD1042, HUD1930, and HUDRHO41U.
MedlineNov 21, 2025 - Lower riskMedical device
Medline Industries, LP recalls SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Medline recalls sterile 5.5" scissors with weak packaging seals that could breach sterility, increasing infection risk. Affected items have specific item numbers and were sold in 2023. Consumers should check labels for item number DYND04000.
MedlineNov 13, 2025 - Use cautionMedical device
Medline Industries, LP recalls DEXLOCK Achilles Repair Implant Kits, MAKT4520
Medline recalls DEXLOCK Achilles Repair Implant Kits (MAKT452:19019) due to drill bit fusing to the bushing during surgery, potentially prolonging procedures.
MedlineNov 11, 2025
Medline Industries, LP recall questions
How many recalls has Medline Industries, LP had?
576 recalls from Medline Industries, LP are on record with U.S. safety agencies, from 2025–2026 (574 medical device, 2 drug).
What is the most recent Medline Industries, LP recall?
Medline Industries, LP recalls Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A, dated Sep 11, 2026. Every Medline Industries, LP recall is listed on this page, newest first.
Why are Medline Industries, LP products recalled?
The most common reasons on record: Unapproved design changes to the products outside of the 510(k) clearance. (17).
What should I do if I have a recalled Medline Industries, LP product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Medline Industries, LP recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.