Manufacturer

Medline Industries, LP

351 recalls in our database name Medline Industries, LP 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.

151–175 of 351

SevereFDA (Devices)·Z-1715-2026·2026-04-15
Medline Angiographic Syringe Adaptor Kits Recalled for Disconnection Risk
Medline Industries is recalling 1,698 medical convenience kits containing angiographic syringe adaptors that may unwind during use, causing loose or disconnected connections between components.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CSTM MANIFOLD KIT - TITUS, Medline SKU VASC1061; 2. CSTM MANIFOLD KIT - FRYE, Medline SKU VASC1074; 3. CRYO EP MANIFOLD KIT, M
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1726-2026·2026-04-15
Medline Syringe Adapter Kits Recalled Due to Potential Disconnection During Use
Medline has recalled medical convenience kits containing rotating syringe adapters that may unwind and disconnect during use, potentially compromising the connection between syringes and manifolds in clinical settings.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ANGIO PACK, Medline SKU # DYNJ57032D; 2. NEURO INTERVENTIONAL RADIOLOGY, Medline SKU # DYNJ64026C; 3. NEURO INERVENTIONAL RADI
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1722-2026·2026-04-15
Medline recalls medical convenience kits with faulty syringe adapters
Medline Industries is recalling medical convenience kits containing syringes with adapters that may unwind during use, potentially causing disconnection from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. LAPAROSCOPIC HERNIORRHAPHY DSC, Medline SKU # DYNJ63021B; 2. LAP PACK, Medline SKU # DYNJ64297B; 3. MINOR PROCEDURE PACK, Medl
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1714-2026·2026-04-15
Medical convenience kits recalled for potential syringe adapter disconnection
Medline recalls 3,120 medical convenience kits containing control syringes due to a potential risk that the rotating adaptor could unwind during use, causing loose or complete disconnection from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: CVOR ANGIOGRAPHY PACK-LF, Medline SKU DYNJ42367B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1716-2026·2026-04-15
Medline Medical Kits with Faulty Syringe Adaptors Pose Disconnection Risk
Medline is recalling medical convenience kits containing syringe adaptors that could loosen or disconnect during catheterization procedures.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. CATH LAB PACK-LF, Medline SKU 00-HCT055P; 2. INTERVENTIONAL CATH LAB PK-LF, Medline SKU DYNJ0376230Q; 3. ANGIOGRAPHY CATH LAB,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1728-2026·2026-04-15
Medline medical convenience kits with defective syringe rotating adaptors recalled
Medline is recalling 439 medical convenience kits worldwide containing defective NAMIC Angiographic RA Control Syringes. The syringe rotating adaptor may unwind during use, causing loose or full disconnection between the syringe and manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. ROBOTIC PACK, Medline SKU # DYNJ58475F; 2. URO/GEN ROBOTIC PACK, Medline SKU # DYNJ60803J.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1712-2026·2026-04-15
NAMIC Angiographic Syringes May Disconnect Due to Adaptor Failure
NAMIC Angiographic Syringes may have rotating adaptors that unwind during use, causing loose or complete disconnection from the manifold, affecting 2.6 million units distributed worldwide.
Product
NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2. SYRINGE,10ML,TR/FR,RA,W/RES, Medline SKU 70085007; 3. MTO,SYRINGE,10ML,TR/FG,RA,-,PKG, Medline SKU 70085107; 4. SYRINGE,12ML,TR/FR,RA,W/RES, Medline SKU 70087007; 5.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1713-2026·2026-04-15
NAMIC Angiographic Control Syringes recalled for potential adapter disconnection
Medline's NAMIC Angiographic Control Syringes are being recalled because the rotating adaptor may unwind during use, potentially causing disconnection from the manifold. This Class I recall affects 192,690 units distributed worldwide.
Product
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OE
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2026·2026-04-08
Medline Biopsy Valve Kits Recalled for Risk of Rubber Fragment Detachment
Medline has recalled 14,379 biopsy valve kits due to complaints about rubber fragments detaching from the valve slit. These fragments could lodge in a patient's airway and may require removal intervention.
Product
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2026·2026-04-08
Medline Bronchoscopy Kits Recalled for Rubber Fragment Detachment Risk
Medline is recalling 14,379 kits containing Olympus biopsy valves due to rubber fragments that may detach and lodge in a patient's airway. The detachment may require surgical removal and could cause inflammation or reduced oxygen levels.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1710-2026·2026-04-08
Medical procedure kits with defective biopsy valves recalled
Medline is recalling 14,379 surgical procedure kits containing Olympus biopsy valves that may shed rubber fragments during use, potentially creating airway obstruction.
Product
Medline kits containing Olympus biopsy valves: 1. BRONCH PROCEDURE KIT, DYKE2091 2. BRONCHSCOPY, DYNJ900898G DYNJ901922I 3. BRONCHSCOPY PACK, DYNJ38313B 4. BRONCHOSCOPY PACK 0120367-LF, DYNJ32750G DYNJ32750I 5. KIT, WR THORACIC, DYNJ911252 6. LARYNGOSCOPY/BRON
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1693-2026·2026-04-08
Sterile Radiology Procedure Kits Recalled for Potential Packaging Sterility Breach
Medline Industries is recalling 420 units of Sterile Radiology Procedure Kits (Model DYNDH1491B, Lot 25GBB924) due to a potential breach in sterile pouch packaging that may compromise product sterility.
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1705-2026·2026-04-08
Medline Airway Exam Kit Recalled for Rubber Fragment Detachment Risk
Medline's Airway Exam Kit (DYKE1796) is being recalled due to a defect in included Olympus biopsy valves. Rubber fragments may detach into the patient's airway, potentially requiring emergency intervention.
Product
Airway Exam Kit, DYKE1796
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFIT G-Tube Connector Recalled for Defective Seal Formation Risk
Medline is recalling 651,789 ENFIT G-Tube Connectors because they may not form a proper seal with compatible feeding devices, risking leakage that could delay care and cause fluid loss.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2026·2026-04-08
Medline ENFIT G-Tube Connector Kits Recalled for Seal Defects
Medline recalls 9,040 ENFIT G-tube connector kits due to manufacturing defects preventing proper sealing and causing leakage, risking delayed care. Over-tightening to prevent leakage risks infection and additional clinical complications.
Product
Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1707-2026·2026-04-08
Thoracic Biopsy Valve Kits Recalled Due to Rubber Fragment Detachment
Medline Industries is recalling 14,379 thoracic biopsy valve kits due to rubber fragment detachment in Olympus biopsy valves. Fragments may lodge in the airway and require medical intervention.
Product
THORACIC ROBOTS, DYNJ908777B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1706-2026·2026-04-08
Medline Bronchoscopy Kits Recalled for Rubber Fragment Risk in Biopsy Valves
Medline convenience kits containing Olympus biopsy valves are being recalled due to rubber fragments detaching from the valve slit. This could create a foreign body in a patient's airway, potentially requiring removal and causing breathing complications.
Product
Medline convenience kits containing Olympus biopsy valves: 1. BRONCH PACK, DYKE2096 2. NON MB BRONCHOPSCOPY CCH LH PK, DYNJT6182 3. PULMONARY BRONCH PACK, DYNDA2861A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1711-2026·2026-04-08
Medline Anterior Hip Pack with defective biopsy valves recalled
Medline is recalling hip surgery kits containing Olympus biopsy valves with a defect that can cause rubber fragments to detach. These fragments pose a risk of lodging in the patient's airway.
Product
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1650-2026·2026-04-01
Puracol and Puracol Plus Collagen Wound Dressings Recalled for Elevated Endotoxin Levels
Medline Industries is recalling Puracol and Puracol Plus Collagen Wound Dressings due to elevated endotoxin levels. Affected products may cause tissue irritation, delayed healing, or in severe cases, septic shock.
Product
Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1564-2026·2026-03-18
Medline Surgical Drapes Recalled Due to Premature Fabric Delamination
Medline Industries is recalling surgical drapes that may develop premature fabric delamination during laundering. This could delay patient care or allow surgical site contamination if the affected product is used.
Product
Medline Surgical Drapes: MDTBTCS6070GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTBTCS6090GN DBD-DRAPE,COVER,TABLE,RESIS/XALT GRN,60X MDTDXUNDBGN DBD-DRAPE,UNDERBUTTOCK,28 X 50.5,XALT GR MDTMAYOXGN DBD-DRAPE,COVER,MAYO STAND,RESISTAT/XALT MDTZ1003656GN DBD-POCKET SHEET,RESISTAT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2026·2026-03-18
Medline Medcrest Surgical Gowns Prone to Premature Fabric Delamination
Medline Medcrest surgical gowns may delaminate when laundered, risking surgical barrier failure and infection. The FDA has recalled 104,004 units distributed nationwide and internationally.
Product
Medline Medcrest Surgical Gowns: MDTGXC4J5XL DBQ-GOWN,SURG,XALT,L4, CRTCL CVR, GRN, 5 MDTGXC4JL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,L MDTGXC4JXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XL MDTGXC4JXXL DBD-GOWN,SURG,XALT,L4,CRTCL CVR,GREEN,XX MDTGXP4JL DBD-GOWN,SURG,XALT,L4,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1562-2026·2026-03-18
Medline Chest Drainage Units: Instructions Clarified for Adult Use Only
Medline is clarifying instructions for Aqua-Seal Chest Drainage Units to specify they are intended for adults 18 years and older. Approximately 2,894 units distributed worldwide are affected.
Product
Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2) CARDIAC PROCEDURE, Model Number: DYNJ908126; 3) CARDIO CONGENITO, Model Number: DYNJ910851
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1432-2026·2026-03-04
Medline Nail Kit Recalled for Sterile Wound Wash Sterility Deficiency
Medline is recalling 1,640 Nail Kits containing sterile saline wound wash because the manufacturer may not have met minimum sterility assurance levels. The affected kits were distributed nationwide and internationally.
Product
Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2026·2026-03-04
Medline Tego Connector Kits Recalled for Silicone Seal Defects
Medline is recalling 1,212 units of kits containing Tego Connectors due to silicone seal defects that may block fluid flow, cause therapy delays, or allow air and biological contaminants to enter the body. No illnesses have been reported.
Product
Medline kits containing Tego Connectors Medline APHERESIS SUBQPORT ACCESS KIT SKU DYNDA2705 Medline CENTRAL LINE INSERTION SKU DYNJ63347A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1435-2026·2026-03-04
Meijer Saline Wound Wash Recalled Due to Sterility Assurance Level Failure
Medline Industries is recalling Meijer STERILE saline wound wash because the manufacturer may not have met required sterility standards. The recalled product was distributed nationwide in the US and internationally.
Product
Meijer STERILE saline wound wash, First Aid Cleansing Spray, 0.9% USP SODIUM CHLORIDE, 7.1FL OZ (210 mL), DBD-CAN,SPRAY,7.1-OZ,SALINE,WOUND WASH,S, Model Number MJSALINE7
Category
Medical Device
Distribution
Distributed nationwide