Manufacturer

MEDLINE INDUSTRIES, LP - Northfield

787 recalls in our database name MEDLINE INDUSTRIES, LP - Northfield as the manufacturing or recalling firm.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–25 of 787

SevereFDA (Devices)·Z-2567-2025·2025-10-01
Medline Medical Kits Recalled for Laryngoscope Light Failure
Medline Industries is recalling medical convenience kits containing defective Flexicare BritePro Solo Fiber Optic Laryngoscope Handles that fail to illuminate. The 596 affected units were distributed to healthcare facilities in six U.S. states.
Product
Medline medical convenience kits labeled as: 1. NEWBORN RESUSCITATION KIT, Kit Number ACC010381C; 2. DRAWER 5 - POSITION 3, Kit Number ACC010532; 3. DRAWER #4C ADULT, Kit Number ACC010671; 4. DRAWER #2, Kit Number ACC010728.
Category
Medical Device
Distribution
6 states
SevereFDA (Devices)·Z-2566-2025·2025-10-01
Medline intubation kit laryngoscope handles recalled for light illumination failure
Medline is recalling specific intubation kits with Flexicare BritePro Solo Fiber Optic Laryngoscope Handles due to light illumination failure. The handles may not illuminate properly, potentially affecting visibility during intubation procedures.
Product
Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number ACC010392; 4. INTUBATION KIT, Kit Number ACC010467A; 5. ADULT AIRWAY TRAY, Kit Number ACC01
Category
Medical Device
Distribution
6 states
SevereFDA (Devices)·Z-2460-2025·2025-09-03
Medline ReNewal Reprocessed Electrophysiology Catheters May Contain Residual Particulates
Medline ReNewal reprocessed electrophysiology catheters may contain small residual particulates. The catheters were distributed nationwide to healthcare facilities.
Product
Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH, 401210RH, 401211RH, 401212RH, 401222RH, 401223RH, 401226RH, 401227RH, 401228RH, 401260RH, 401261RH, 401271RH, 401305RH, 401306RH, 401309RH
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0602-2025·2025-09-03
Walmart isopropyl alcohol swabs recalled due to subpotent formulation
Medline Industries is recalling Walmart ReliOn sterile alcohol swabs due to isopropyl alcohol concentrations below the labeled amount. The nationwide recall affects approximately 3.5 million swabs.
Product
WALMART — WALMART (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2479-2025·2025-09-03
Medline Surgical Kits Recalled for Incorrect Foley Tray Information
Medline surgical kits containing BD SureStep Foley Tray Systems have been recalled due to incorrect product information insert sheets that could lead to patient injury, including infection or allergic reaction.
Product
Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DYNJG901001B CRANIOTOMY DYNJ908819B KIT CRANIOTOMY (only units from SKU DYNJG001004A LAVH MINOR were distributed)
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-2452-2025·2025-09-03
Medline General Surgery Tray kits recalled for tourniquet cuff weld defect
Medline is recalling surgical tray kits containing Stryker tourniquet cuffs that may fail due to a manufacturing defect at the weld, risking patient hemorrhaging.
Product
The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utilizing them. The kit is provided sterile, single-use and includes a range of components dependent upon the specific procedure. These kits will be assembled using
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0603-2025·2025-09-03
Sterile Alcohol Pads Recalled for Subpotent Isopropyl Alcohol Concentration
H-E-B inControl sterile alcohol pads are being recalled nationwide because the isopropyl alcohol concentration falls below the labeled amount. Affected consumers should discontinue use.
Product
INCONTROL ALCOHOL — INCONTROL ALCOHOL (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0604-2025·2025-09-03
Antiseptic prep pads recalled for subpotent isopropyl alcohol
Good Neighbor Pharmacy Alcohol Antiseptic Skin Cleanser prep pads are recalled because the isopropyl alcohol concentration is below the labeled amount. Approximately 66,000 pads distributed nationwide are affected.
Product
GOOD NEIGHBOR PHARMACY ALCOHOL ANTISEPTIC SKIN CLEANSER — GOOD NEIGHBOR PHARMACY ALCOHOL ANTISEPTIC SKIN CLEANSER (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0600-2025·2025-09-03
Medline Alcohol Prep Pads recalled for subpotent isopropyl alcohol concentration
Medline Alcohol Prep Pads are being recalled nationwide because the isopropyl alcohol concentration is below the labeled amount, reducing product effectiveness.
Product
MEDLINE ALCOHOL PREP — MEDLINE ALCOHOL PREP (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0605-2025·2025-09-03
Rite Aid Isopropyl Alcohol Prep Pads Recalled for Below-Labeled Concentration
Rite Aid pharmacy isopropyl alcohol prep pads distributed nationwide are being recalled because the alcohol concentration falls below the labeled level. The FDA classified this Class II recall because reduced potency may affect the product's antimicrobial effectiveness.
Product
ALCOHOL — ALCOHOL (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0601-2025·2025-09-03
CURAD Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol
Medline Industries recalls 1,639,996 CURAD Alcohol Prep Pads nationwide because isopropyl alcohol levels fall below the labeled concentration, reducing product effectiveness.
Product
CURAD ALCOHOL PREP PADS — CURAD ALCOHOL PREP PADS (ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2199-2025·2025-08-06
SwabFlush Prefilled Syringe with Faulty Disinfecting Cap Poses Infection Risk
Defective SwabCaps on SwabFlush prefilled syringes may reduce disinfection of luer access valves, potentially causing patient infection. The recall affects 1,427,100 units distributed nationwide and internationally.
Product
SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2156-2025·2025-07-30
Medline Convenience Kits Recalled for Potential Sterility Breach Risk
Medline Convenience Kits containing BD ChloraPrep Clear applicators are recalled due to potential open seals on packaging that may compromise sterility and lead to infection risk during surgical procedures.
Product
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: C-SECTION PREP, REF DYNJ32702B
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2154-2025·2025-07-30
Medline Convenience Kits with BD ChloraPrep Applicators Recalled Over Sterility Concerns
Medline Convenience Kits containing BD ChloraPrep Clear applicators are being recalled due to potential open seals in packaging that could compromise sterility and lead to infection.
Product
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: IV START KIT LAB DRAW-SH, REF CDS860014P
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2153-2025·2025-07-30
Medline Convenience Kits with BD ChloraPrep recalled due to sterility breach risk
Medline Convenience Kits containing BD ChloraPrep applicators are being recalled due to potential open seals that could breach sterility and increase infection risk. The recall affects 960 units distributed in California, Florida, Pennsylvania, and Texas.
Product
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2155-2025·2025-07-30
Medline Convenience Kits with BD ChloraPrep Recalled for Open Seal
Medline Convenience Kits containing BD ChloraPrep applicators are recalled for potential open seals that breach sterility and may cause patient infection. The 15,700 affected units were distributed to California, Florida, Pennsylvania, and Texas.
Product
Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: 1) BLOOD CULTURE KIT, REF DYNDH1462B; 2) BLOOD CULTURE KIT, REF DYNDH1622C; 3) BLOOD CULTR KT DIVRSN DEVICE, REF DYNDH1866.
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-2045-2025·2025-07-09
Medline IV Catheter Kits Recalled for Needle Retraction Failure
Medline is recalling specific convenience kits containing BD Insyte Autoguard IV catheters because the needle may be slow to retract or fail to retract during insertion, posing a potential injury risk.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: RETINAL PACK-LF, REF DYNJ0151148B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2044-2025·2025-07-09
Medline IV Catheter Kits Recalled Due to Needle Retraction Failure
Medline recalls IV catheter convenience kits where the needle is slow to retract or fails to retract during insertion. The affected kits (36 units, Lot 24LDA590) were distributed across six states.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: IV START BOX, REF ACC010665
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2043-2025·2025-07-09
IV Catheters in Medline Kits May Fail to Retract During Insertion
Medline is recalling IV catheters in convenience kits because the needle may be slow to retract or fail to retract during insertion. 186 units were distributed nationwide in six states.
Product
Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER 4 IV CIRCULATION, REF ACC010254B; 2) CC ADULT DRAWER 2, REF ACC010256; 3) PEDI EMERGENCY TRAY-BLUE, REF ACC010316A; 4) ADULT DRAWER 4, REF ACC010389C;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1995-2025·2025-07-02
Medline umbilical catheter tray recalled for outer packaging defect
Medline is recalling its UMBILICAL TRAY W/3.5&5FR CATH due to a possible packaging defect in the outer Tyvek pouch. The defect could compromise the sterile protection of the product.
Product
Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1810-2025·2025-06-11
Medline Codman Craniotomy Perforators Recalled for Inadequate Welds
Medline has recalled 1,853 surgical perforators used in craniotomy procedures due to inadequate welds that may cause the device to break or separate. The affected kits were distributed across 13 US states.
Product
Medline Kits containing Codman Disposable Perforator 14 mm: CRANIOTOMY, SKU DYNJ35349C
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1809-2025·2025-06-11
Medline surgical kits recalled for faulty perforator welds
Medline is recalling surgical kits containing Codman Disposable Perforators due to inadequate welds on specific lots. Affected perforators may break or separate during craniotomy procedures.
Product
Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS983611N 3. CRANIOTOMY CDS, SKU CDS983467J 4. CRANIOTOMY PACK, SKU DYNJ85807A, DYNJ85927 5. MAJOR CRANIOTOMY PACK, SKU DYNJ82007A
Category
Medical Device
Distribution
13 states
SevereFDA (Devices)·Z-1811-2025·2025-06-11
Medline surgical kits recalled for inadequate welds in perforators
Medline is recalling surgical kits containing Codman Disposable Perforators due to inadequate welds that may cause the instruments to break or separate during use.
Product
Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ACCESSORY PACK SKU DYNJ59270 2. CRANI PACK-LF SKU DYNJ44805M 3. CRANIOTOMY SKU CDS982719V CDS982719W DYNJ904168F DYNJ908404B DYNJ908723A DYNJ908723C 4. CRANIOTOMY #IMF 56646-LF SKU DYN
Category
Medical Device
Distribution
13 states
HighFDA (Devices)·Z-1766-2025·2025-05-21
Medline Centurion Sterile Weitlaner Retractor Recalled Due to Packaging Defect
Medline is recalling 840 units of Centurion Sterile Weitlaner Retractors because the sterile packaging could be punctured, potentially compromising device sterility.
Product
Centurion Sterile Weitlaner Retractor 3 x 4 Prong, Reorder: I68395
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1765-2025·2025-05-21
Centurion Sterile Weitlaner Retractor Recalled Due to Sterile Packaging Puncture Risk
Medline Industries recalls 2,100 units of Centurion Sterile Weitlaner Retractors due to potential punctures in sterile packaging that could compromise device sterility. Check lot numbers against the FDA list.
Product
Centurion Sterile Weitlaner Retractor, Reorder: 67315
Category
Medical Device
Distribution
Distributed nationwide