Every recall we track for MEDLINE INDUSTRIES, LP - Northfield — 822 in all — plus the complaints and injury reports the public filed about them.
Medline recalls newborn resuscitation kits and medical drawers with faulty laryngoscope handles that don't illuminate properly. Affected kits have specific kit numbers and lot numbers.
Medline recalls specific intubation trays due to light failure in Flexicare BritePro Solo Fiber Optic Laryngoscope Handles. Affected kits include adult intubation trays with kit numbers ACC010369B through DYNJAA245A.
Medline recalls kits containing BD SureStep Foley trays with mislabeled product sheets. Using these may cause minor injury or medical issues like infection or allergic reactions.
Medline recalls specific lots of reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheters due to potential small residual particulates that could cause injury during medical procedures.
Medline recalls specific surgery trays due to potential tourniquet cuff detachment causing bleeding risks. Affected kits include SKUs CDS983907M, CDS983907N, DYNJ69405B, etc. with specific lot numbers.
Medline Industries recalls 100-pad alcohol pads sold in H-E-B and inControl stores due to subpotent isopropyl alcohol levels below labeled concentration. Consumers should check product details and contact Medline for remedies.
Medline Industries recalls Rite Aid alcohol prep pads due to isopropyl alcohol levels below labeled concentration. Consumers should check product labels for NDC 11822-5156-2 or 61224070083.
Medline recalls 100-count alcohol prep pads due to isopropyl alcohol levels falling below labeled concentration. Consumers should check product details and contact Medline for guidance.
Medline Industries recalls ReliOn Sterile Alcohol Swabs due to isopropyl alcohol levels below labeled concentration. Consumers should check product details and contact Medline for remedy.
Curad recalls sterile alcohol prep pads due to isopropyl alcohol levels below labeled concentration. This may reduce effectiveness for disinfection. Consumers should check product details and contact Medline for guidance.
Medline Industries recalls Good Neighbor Pharmacy Alcohol Prep Pads due to subpotent isopropyl alcohol levels below labeled concentration. Consumers should check product details and contact Medline for guidance.
Medline recalls SwabFlush Prefilled Syringes with ICU Medical SwabCaps due to a seal issue that may reduce disinfection, risking patient infection. Affected units include specific model numbers and lots.
Medline recalls Labor Triage Kits with BD ChloraPrep Clear applicators due to potential open packaging that could breach sterility, risking infection. Affected kits have specific lot numbers and reference codes.
Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators due to potential open seals causing sterility breaches. Affected kits may lead to patient infections if used.
Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators due to potential open packaging that could breach sterility, risking patient infection.
Medline recalls convenience kits with BD ChloraPrep Clear 1mL applicators that may have open packaging, risking sterility breaches and patient infections. Affected kits include specific blood culture kit references and lot numbers.
Medline recalls convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN labeled RETINAL. The catheters may slow or fail to retract during insertion, potentially causing injury.
Medline recalls specific IV kits containing BD Insyte Autoguard Shielded IV Catheters that may slow or fail to retract during insertion, risking injury. Affected kits have unique identifiers.
Medline recalls convenience kits containing specific BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN that may cause slow or failed needle retraction during insertion. Affected kits have unique lot numbers and labels.
Medline recalls umbilical trays with possible packaging defects that could compromise sterile product protection. Affected units include specific lot numbers and model UVT1250.
Medline recalls specific kits containing Codman Disposable Perforators with inadequate welds that may break or separate. Affected kits include CRANI ACCESSORY PACK and CRANI PACK-LF models. Stop using immediately.
Medline recalls craniotomy kits with Codman Disposable Perforators that may break due to inadequate welds. Affected kits have specific SKUs and lots. Stop using immediately to prevent injury.
Medline recalls surgical kits containing Codman Disposable Perforators 14mm with inadequate welds that may break or separate during use.
Medline recalls Centurion Sterile Weitlaner retractors that may puncture sterile packaging. Affected units have specific lot numbers and UDI/DI codes. Stop using and contact Medline for replacement.
Medline recalls Centurion Sterile Weitlaner Retractor 3x4 Prong models with specific lot numbers due to potential puncture through sterile packaging. Affected users should check their product details.
Meridian Bioscience recalls specific lot of ImmunoCard STAT! Crypto/Giardia Test Kits (Model 750830) due to improper storage temperature. This may affect test accuracy but does not pose immediate safety risks.
Medline procedure kits with leaking sterile water or saline bottles recalled due to peel-foil interface issues. Affected kits have specific model and lot numbers.
Medline recalls non-sterile I&D kits with leaking sterile water and saline bottles. Affected kits have specific model numbers and lot codes. Stop using immediately to prevent contamination risks.
Medline recalls wound care and laceration trays with leaking sterile water and saline bottles. Affected units have specific model numbers and lot codes. Stop using immediately to prevent contamination.
Medline recalls procedure kits with leaking sterile water and saline bottles that could contaminate surgical tools. Affected kits have specific lot numbers and model references.
Medline recalls procedure kits labeled OL OCULAR with leaking sterile water and saline bottles. Affected kits may cause contamination if used improperly. Contact Medline for replacement.
Medline recalls procedure kits labeled REDDY JOINT BATH (REF MMJB001A) due to leaking sterile water and saline bottles. Affected kits may cause contamination if used improperly.
Medline Sterile Water 100mL bottles (ref RDI30295) may leak at the peel-foil interface. Recalled due to potential contamination risks. Return or stop use if you have these specific lot numbers.
Medline Sterile 0.9% Normal Saline bottles (100mL) with specific lot numbers leak at the peel-foil interface. Recalled to prevent contamination and potential infection risks.
Medline recalls sterile procedure kits with leaking bottles that could cause contamination. Affected kits include Sterile Prep Kit (DYNDA1359A) and others. Stop using immediately to avoid infection risks.
Medline recalls procedure kits (T AND A PACK -LF, REF DYNJ85792) due to leaking sterile water and saline bottles. Affected kits may cause contamination if used.
Medline Renewal recalls ENT Coblator II ProCise Max devices with specific lot numbers due to risk of drip chambers disconnecting from saline tubing when under tension.
Medline recalls ReNewal Coblator II Evac 70 Xtra Plasma Wands with potential drip chamber disconnection under tension. Affected units have specific lot numbers and item numbers. Stop using immediately to prevent saline line disconnection.
Medline recalls ENT devices with serial numbers 513993-532817 that may disconnect under tension, risking fluid leaks during surgery.
Medline Renewal recalls ENT Coblator II PROcise XP Wand with integrated suction and saline. Drip chambers may disconnect from saline tubing when under tension, potentially causing saline flow issues during use.
Medline recalls 37 convenience kits for cardiac procedures due to potential weak seals on breather pouches that could lead to contamination. Affected kits include specific models and lot numbers.
Medline recalls convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Affected kits include PRECIP TRAY model MNS12590.
Medline recalls intubation tray kits (model MNS10395) due to potential weak seals on breather pouches that could lead to contamination during procedures.
Medline recalls two pain kits (DYNJ67577A and DYNJ67576A) due to potential open/weak seals on breather pouches, which could compromise sterility during medical procedures.
Medline recalls 31 convenience kits for eye procedures due to potential weak seals on breather pouches that could lead to contamination. Kits with specific model numbers and lot numbers are affected.
Medline recalls 20 convenience kits for medical procedures due to potential weak seals on breather pouches that could lead to contamination. Affected kits include Angiography Drape Packs and others with specific model numbers and lot dates.
Medline recalls 170 specific breather pouch models used in sterile medical kits due to potential open or weak seals that could compromise sterility.
Medline recalls Rhino Plasty Pack convenience kits (model DYNJ27333F) due to potential weak seals on breather pouches that could lead to contamination during procedures.
Medline recalls 24 types of convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Affected kits include OB packs, D&C packs, and others with specific model numbers and lot numbers.
Medline recalls specific convenience kits for gynecological and hysteroscopy procedures due to potential weak seals on breather pouches that could lead to contamination.
Medline Industries recalls 121 batches of breather pouches used in sterile convenience kits due to potential open/weak seals that could compromise sterility.
Medline recalls specific convenience kits for procedures due to potential weak seals on breather pouches that could lead to contamination. Affected kits include large biopsy packs and soft tissue biopsy packs with model numbers starting with DYNJ.
Medline recalls hernia repair tote kits with potential weak seals on breather pouches that could compromise sterility during surgery.
Medline recalls Universal Drape Pack (Model DYNJCD0239) due to potential weak seals on breather pouches that could compromise sterile packaging.
Medline recalls IV Pack South convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures.
Medline recalls convenience kits with weak breather pouch seals that may allow contamination. Affected kits include CSTM PACEMAKER DRA: DYNJCD0339 model. Stop using immediately to prevent infection risks.
Medline recalls 80+ ENT/Head and Neck convenience kits with potentially weak seals on breather pouches that could lead to contamination during procedures.
Medline recalls 33 convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Check model numbers and lot numbers for affected items.
Medline recalls 16 types of sterile convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures.
Medline recalls three convenience kits with potential weak seals on breather pouches that could lead to contamination during medical procedures. Affected kits include ANGIO CONSOLIDATED PACK (DYNJHTCAD1) and others. Consumers should check model numbers and lot dates.
