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Recall archive

95,388 stored notices, from Jun 20, 2012 to Nov 11, 2026.

126 recalls · page 2 of 6

Medical devices

Reported Apr 15, 2026

NAMIC Angiographic Syringe, labeled as follows: 1. SYRINGE,20ML,CONTROL,-,PKG, Medline SKU 70075027; 2.…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which…

18 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details — Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to…

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2026

Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand — Elevated endotoxin levels identified in affected lots. Issue may elicit strong inflammatory response if used, including local tissue irritation,…

FDA (openFDA device enforcement)

Medical devices

Reported Mar 18, 2026

Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit: 1) OPEN HEART, Model Number: DYNJ902487A; 2)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details — The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended…

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 4, 2026

Medline Sterile Saline Wound Wash, Cleansing & Wound Irrigation, USP Normal Saline (0.9% Sodium Chloride), 7.1 FL OZ…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline has identified that the manufacturer of the sterile saline wound wash may not have manufactured products to meet the minimum required…

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 25, 2026

Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET,60DRP,1NEEDLE-FREE VALV, Model Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details — Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration…

42 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 18, 2026

Medline 14 Fr Suction Catheter Kits SKU DYND40972 - respiratory convenience kit

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details — A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use…

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 4, 2026

Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing…

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 28, 2026

MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as…

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 21, 2026

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: AN01 CAROTID ANESTH…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the…

17 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 14, 2026

Medline Hudson RCI Medium Concentration Oxygen Masks: 1041CE MASK,OXYGEN,UND CHIN,MED CO OUS ONLY; HUD1035 O2 MASK,MED…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details — Firm received multiple complaints regarding tubing disconnecting from oxygen mask. If issue occurs during use, may lead to delay in patient care and…

FDA (openFDA device enforcement)

Medical devices

Reported Dec 24, 2025

SCISSORS, OR, SHARP/BLUNT, 5.5", STERILE, Item Number DYND04000

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand — The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if…

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 17, 2025

MEDLINE PERFUSION SYRINGE, REF: DYNJ39223C

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing BD Luer Tip Caps. BD has issued a recall of…

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 26, 2025

MEDLINE STERILE BASIC EYE PACK 16: 1) REF: DYNJ37743D; 2) REF: DYNJ37743F.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Medline has identified specific sterile eye procedure kits with pouch packaging that may exhibit open seals.

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 19, 2025

Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; Product description/Product numbers:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

Matched: Brand — Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to…

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 29, 2025

Excelsior Medical, 0.9% Sodium Chloride Injection, USP - 10 mL Fill, Item Number EMZ111240. Prefilled saline flush…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Reason for recall — Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 22, 2025

Medline Adult Anesthesia Set, REF DYNJ39985G

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medline Industries, LP

Matched: Brand · Product · Product details · Reason for recall — Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 8, 2025

Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medline Industries, LP

Matched: Brand · Product · Product details — Convenience kits labeled as sterile have not gone through the sterilization process.

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2025

Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

MEDLINE INDUSTRIES, LP - Northfield

Matched: Brand · Product · Product details · Reason for recall — Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Flexicare BritePro Solo Fiber Optic…

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Oct 1, 2025

READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle,…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Medline Industries, LP

Matched: Brand · Product details — Subpotent drug

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 3, 2025

The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

Matched: Brand · Product · Product details — Affected kits contain recalled Stryker Color Cuff Sterile Disposable Tourniquet Cuffs. Stryker Instruments initiated this recall due to a potential…

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

Matched: Brand — SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal…

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

Matched: Brand · Product · Product details — Affected convenience kits contain BD ChloraPrep Clear - 1 mL Applicators, which were recalled by BD due to potential to exhibit an open seal on its…

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 9, 2025

Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

MEDLINE INDUSTRIES, LP - Northfield

Matched: Brand · Product · Product details · Reason for recall — Medline Industries, LP. is issuing a recall for specific Medline kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN which was…

2 more products in this recall

FDA (openFDA device enforcement)

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