Manufacturer

Medline Industries, LP

534 recalls in our database name Medline Industries, LP as the manufacturing or recalling firm.

What the numbers show

Total: 534
Critical: 38
Severe: 92
Most recent: 2026-09-09

Of the 534 recalls from Medline Industries, LP we have scored against our rubric, 38 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 92 (17%) are Severe.

Which agencies issued them

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.

326–350 of 534

SevereFDA (Devices)·Z-1715-2026·2026-04-15
Medline custom manifold kits recalled over syringe adaptor unwinding risk
Medline is recalling custom manifold and cryo EP manifold kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 1,698 kits are affected.
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-1730-2026·2026-04-15
Medline arthroscopy and extremity packs recalled over syringe adaptor unwinding
Medline is recalling Shoulder Arthroscopy and Extremity Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. SHOULDER ARTHROSCOPY PACK, Medline SKU # DYNJ30880M; 2. EXTREMITY PACK, Medline SKU # DYNJ64295A.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1726-2026·2026-04-15
Medline angiography and neuro kits recalled over syringe adaptor disconnection
Medline is recalling Angio Pack and Neuro Interventional Radiology convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
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-1721-2026·2026-04-15
Medline head, neck and heart cath packs recalled over syringe adaptor defect
Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K; 2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 3. HEART CATH PACK-LF, Medlin
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1722-2026·2026-04-15
Medline laparoscopic and minor procedure packs recalled over syringe adaptor defect
Medline is recalling laparoscopic herniorrhaphy, lap and minor procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
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-1723-2026·2026-04-15
Medline minor plastic surgery packs recalled over syringe adaptor unwinding risk
Medline is recalling Minor Plastic-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: MINOR PLASTIC-LF, Medline Kit SKU # DYNJ86596
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1720-2026·2026-04-15
Medline special procedure trays recalled over syringe adaptor disconnection risk
Medline is recalling Special Procedure Trays containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 762 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: SPECIAL PROCEDURE TRAY, Medline SKU # DYNJ80513B
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1717-2026·2026-04-15
Additional NAMIC angiographic syringe lots recalled over adaptor unwinding
Medline is recalling a further group of NAMIC Angiographic Syringe lots because the rotating adaptor can unwind during use and disconnect from the manifold. 149,439 units are affected.
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. MTO,SYRING
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1712-2026·2026-04-15
NAMIC syringe recall reaches 2.6 million units over adaptor unwinding defect
Medline is recalling a further tranche of NAMIC Angiographic Syringes because the rotating adaptor can unwind during use and disconnect from the manifold. 2,630,369 units are affected.
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-1724-2026·2026-04-15
Medline cardiac catheterization kits recalled over syringe adaptor unwinding
Medline is recalling right and left heart catheterization and angiography kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 79,843 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. MTS RH LFT HRT KIT, Medline SKU # 60010508; 2. MTS 3V W/GUIDE, Medline SKU # 60100701; 3. ANGIOGRAPHY KIT, Medline SKU # 60131
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1713-2026·2026-04-15
NAMIC angiographic control syringes recalled over rotating adaptor unwinding
Medline is recalling NAMIC Angiographic Control Syringes because the rotating adaptor can unwind during use, causing a loose connection or full disconnection from the manifold. 192,690 units are affected.
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
SevereFDA (Devices)·Z-1727-2026·2026-04-15
Medline delivery packs recalled over syringe rotating adaptor disconnection risk
Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. DELIVERY PACK, Medline SKU # DYNJ42892F; 2. DELIVERY PACK, Medline SKU # DYNJ42892G.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1729-2026·2026-04-15
Medline TAVR procedure packs recalled over syringe adaptor disconnection risk
Medline is recalling TAVR PACK convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 108 units are affected.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: TAVR PACK, Medline SKU # DYNJ84472
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1719-2026·2026-04-15
Medline non-vascular and vein packs recalled over syringe adaptor defect
Medline is recalling Non Vascular Pack and Vein convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1725-2026·2026-04-15
Medline glove pack kits recalled over syringe adaptor disconnection risk
Medline is recalling GLOVE PACK 7.0 convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Product
Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: GLOVE PACK 7.0 (15PK), Medline SKU # DYNJ63673D
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1718-2026·2026-04-15
NAMIC angiographic syringes recalled in the largest rotating adaptor action
Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.
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. MTO,SYRING
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1705-2026·2026-04-08
Airway exam kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling the Airway Exam Kit because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Airway Exam Kit, DYKE1796
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1710-2026·2026-04-08
Medline bronchoscopy kits contain Olympus biopsy valves that shed fragments
Medline is recalling six bronchoscopy and thoracic kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
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-1711-2026·2026-04-08
Medline anterior hip pack contains recalled Olympus biopsy valves
Medline is recalling the Anterior Hip Pack because it contains recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
MEDLINE ANTERIOR HIP PACK DYNJ64672B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1693-2026·2026-04-08
Sterile radiology procedure kits may have a breached sterile pouch
One lot of Sterile Radiology Procedure Kits, model DYNDH1491B, is being recalled because of a potential breach in the sterile pouch packaging that may compromise sterility.
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2026·2026-04-08
Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments
Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
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-1707-2026·2026-04-08
Medline thoracic robot kits contain recalled Olympus biopsy valves
Medline is recalling Thoracic Robots kits, model DYNJ908777B, because they contain recalled Olympus biopsy valves where rubber fragments may detach from the valve slit.
Product
THORACIC ROBOTS, DYNJ908777B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1706-2026·2026-04-08
Medline bronchoscopy packs contain recalled Olympus biopsy valves shedding fragments
Medline is recalling three bronchoscopy convenience kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
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-1708-2026·2026-04-08
Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Category
Medical Device
Distribution
Distributed nationwide