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.

276–300 of 351

HighFDA (Devices)·Z-1085-2026·2026-01-21
Medline medical robotics kits recalled for irrigation solution leakage during use
Medline is recalling medical procedure convenience kits containing Stryker Strykeflow 2 Suction Irrigators due to a 2024 design change that allows irrigation solution to leak into the handpiece and battery pack during use.
Product
Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2026·2026-01-21
Medline Surgical Kits with Strykeflow 2 Suction Irrigators Recalled for Leakage
Medline surgical procedure kits containing Stryker Strykeflow 2 Suction Irrigators are recalled because a 2024 design change allows irrigation solution to leak into the handpiece and battery pack, potentially causing leakage or vaporized saline emission during use.
Product
Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1050-2026·2026-01-21
Medline Cardiac Procedure Kits Recalled Due to Stuck Check Valve in IV Administration Sets
Medline has recalled 633 kits containing B. Braun IV Administration Sets and Pump Administration Sets due to customer complaints that check valve components may become stuck in open or closed positions.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) OPEN HEART ACCESSORY CDSKit SKU CDS984289O; 2) OPEN HEART CDSKit SKU CDS984355K; 3) BAG A OPEN HEART KITKit SKU DYKM1025D; 4) RR-CABG SUPPLEMENTAL PACKKit SKU DYNJ0394752
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1052-2026·2026-01-21
Medline IV Administration Kits Recalled Due to Check Valve Malfunction
Medline is recalling IV administration kits containing B. Braun administration sets because check valve components may become stuck in open or closed positions. Ninety-six units were distributed nationwide.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1055-2026·2026-01-21
Medline IV Administration Kits Recalled for Check Valve Malfunction
Medline has recalled multiple kits containing B. Braun IV administration sets because the check valve components may become stuck in open or closed positions. The recall affects 3,045 units distributed nationwide.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DRAWER 2 IV SUPPLIES, Medline kit SKU ACC010271B; 2) DRAWER 2 IV FLUIDS & TUBING, Medline kit SKU ACC010416B; 3) OXYGENATION & TUBING TRAY, Medline kit SKU ACC010525C; 4)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1051-2026·2026-01-21
Medline IV Administration Kits recalled for stuck check valve defect
Medline is recalling certain pre-op kits due to check valve defects in IV and pump administration sets. The valves may become stuck in either position, potentially impairing medication delivery.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1049-2026·2026-01-21
Medline IV Administration Kits Recalled for Check Valve Sticking Risk
Medline is recalling IV administration kits containing B. Braun components due to check valve defects that may become stuck. The kits were distributed nationwide and used in anesthesia procedures.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH KIT-LF, Medline Kit SKU PHS972096014B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1053-2026·2026-01-21
Medline IV Administration Sets Recalled for Stuck Check Valves
Medline Industries is recalling 33 units of IV and pump administration sets due to check valve components that may become stuck in open or closed positions, potentially affecting fluid delivery.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: RR-LAP DONOR NEP ACCESSORY, Medline kit SKU DYNJ63395B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1088-2026·2026-01-21
Medline Surgical Procedure Kits Recalled Due to Irrigation Solution Leakage
Medline is recalling 12,584 surgical procedure kits containing Stryker Strykeflow 2 irrigators due to a design defect that causes irrigation solution to leak and emit vaporized saline during use.
Product
Medline medical procedure convenience kits labeled as: 1) ROBOTIC, REF CDS980523M; 2) ROBOTIC GYN, REF CDS980647K; 3) DAVINCI PROCEDURE, REF CDS980864Q; 4) GYN-URO LAPSCP CDS-LF, REF CDS981583U; 5) GYN-URO LAPSCP CDS-LF, REF CDS981583V; 6) GYN ROBOTIC, REF CDS981826K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1059-2026·2026-01-21
Medline IV Administration Sets Recalled for Stuck Check Valve
Medline has recalled Neuro Angio Packs containing B. Braun IV and pump administration sets because check valve components may become stuck in open or closed positions, potentially affecting medication delivery.
Product
Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1035-2026·2026-01-14
Medline oxygen masks recalled due to tubing disconnection risk
Medline Hudson RCI oxygen masks may experience tubing disconnection during use, potentially delaying patient care and causing hypoxia. The company has received multiple complaints about this defect.
Product
Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED CONC,SHORT,PEDI,7' TUB SC; HUD1042 O2 MASK,MED CONC,PEDI,7' TUB SC; HUD1930 O2 MASK,MED CONC,ADULT,7' TUB UC; HUDRHO41U MASK,OXYGEN,MEDIUM-CONCENTRAT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0922-2026·2025-12-24
Medline Sterile Kelly Forceps Recalled Due to Weak Packaging Seals
Medline is recalling sterile Kelly forceps (Item DYNJ04048) distributed in CA, CO, IL, KS, and MI. Weak packaging seals may compromise sterility, increasing the risk of infection if the product is used.
Product
FORCEP, STD STR, STERILE KELLY, 5.5 IN, Item Number DYNJ04048
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0921-2026·2025-12-24
Medline Surgical Scissors Recalled Due to Weak Packaging Seals
Medline Industries is recalling sterile surgical scissors with Item Number DYND04000 due to weak packaging seals that may breach sterility. If the seal fails, there is an increased risk of infection when the product is used.
Product
SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2026·2025-12-17
DEXLOCK Achilles Repair Implant Kits Drill Bit Fusion Issue
Medline's DEXLOCK Achilles Repair Implant Kits may experience drill bit fusion to the drill guide bushing during surgery, potentially prolonging procedures. 163 units were distributed nationwide.
Product
DEXLOCK Achilles Repair Implant Kits, MAKT4520
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0899-2026·2025-12-17
Medline Curad Quick Strip Bandages Recalled for Open Packaging Seals
Medline is recalling Curad Quick Strip Fabric Bandages (18,000 units) due to open seals that may compromise sterility. Distribution affected: US, Guam, Canada, and United Arab Emirates.
Product
Curad Quick Strip Fabric Bandages Containing 30 Bandages of 3/4" x 3", Medline Item Number CUR1930P
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0886-2026·2025-12-17
Medline Perfusion Syringe Recalled for Failed Biocompatibility Testing
Medline Industries recalled Perfusion Syringes containing BD Luer Tip Caps that failed biocompatibility testing. The caps may cause sensitization, irritation, pyrogenicity, or acute systemic toxicity, though no patient injuries have been reported.
Product
MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0898-2026·2025-12-17
CURAD Germ-Shield Fabric Bandages recalled for potentially compromised sterility
Medline is recalling CURAD Germ-Shield Touch-Free Fabric Bandages because packaging seals may be open, potentially compromising product sterility. Consumers should stop using affected units.
Product
CURAD Germ-Shield Touch-Free Fabric Bandages, Sterile, 0.75" x 3", 30/Box, Medline Item Number CUR1930F
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0902-2026·2025-12-17
Medline Recalls Curad Sterile Adhesive Bandages for Packaging Seal Defects
Medline Industries is recalling Curad Touch-Free and Quick-Strip Sterile Adhesive Bandages due to potential open package seals that could compromise product sterility. Approximately 1.57 million units were distributed in the US, Guam, Canada, and UAE.
Product
Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON256133QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0904-2026·2025-12-17
Medline Quick Strip Fabric Bandages recalled for potentially compromised sterility
Medline is recalling all lots of Quick Strip Fabric Sterile Adhesive Bandages because open packaging seals may compromise product sterility. The recall affects 11,291,800 units.
Product
Quick Strip Fabric Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25660QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0900-2026·2025-12-17
Medline Quick Strip Plastic Bandages Recalled for Potentially Compromised Sterility
Medline is recalling approximately 1.7 million Quick Strip Plastic Sterile Adhesive Bandages due to open packaging seals that may compromise product sterility. Affected products were distributed in the US, Guam, Canada, and UAE.
Product
Quick Strip Plastic Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25500QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0903-2026·2025-12-17
Medline Quick Strip Adhesive Bandages Recall Due to Open Packaging Seals
Medline is recalling Quick Strip Fabric Sterile Adhesive Bandages due to open seals in packaging that may compromise sterility. Approximately 6.9 million units distributed in the US, Guam, Canada, and UAE are affected.
Product
Quick Strip Fabric Sterile Adhesive Bandages, 0.75" x 3", Medline Item Number NON25650QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0901-2026·2025-12-17
Medline Quick Strip Sterile Adhesive Bandages recalled for compromised packaging seals
Medline is recalling all lots of Quick Strip Plastic Sterile Adhesive Bandages (1" x 3") due to open seals in packaging that may compromise sterility. No injuries have been reported.
Product
Quick Strip Plastic Sterile Adhesive Bandages, 1" x 3", Medline Item Number NON25600QS
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-0517-2026·2025-11-26
Medline Smoke Evacuation Pencils Recalled for Unintended Activation Risk
Medline Industries recalls surgical smoke evacuation pencils in convenience kits due to activation hazards. Products may activate without manual input when plugged into power, or remain active after release.
Product
MEDLINE convenience kits labeled as: 1) MAJOR LAPAROTOMY CDS, REF CDS860015W; 2) MAJOR LAPAROTOMY CDS, REF CDS860015X; 3) MINOR LAPAROTOMY CDS, REF CDS860016R; 4) MINOR LAPAROTOMY CDS, REF CDS860016S; 5) LAPAROTOMY CDS #31-RF, REF CDS860062S; 6) LAPAROSCOPY CDS, REF
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0523-2026·2025-11-26
Medline Smoke Evacuation Surgical Pencils Recalled for Unintended Activation Risk
Medline Industries recalls surgical smoke evacuation pencils due to potential for unintended activation when plugged in or failure to deactivate after use, affecting 424 kits nationwide.
Product
MEDLINE convenience kits labeled as: 1) MAJOR VAGINAL HARPER PACK-LF, REF DYNJ0161768G; 2) ACH MAJOR VAGINAL PACK, REF DYNJ67757B.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0525-2026·2025-11-26
Medline smoke evacuation pencils recalled for unintended activation
Medline Industries recalls SafeAir smoke evacuation pencils from surgical kits due to potential unintended activation. The devices may activate without user input when powered on or remain active after buttons are released.
Product
MEDLINE convenience kits labeled as: CIRCUMCISION PACK, REF DYNJ16826O
Category
Medical Device
Distribution
Distributed nationwide