Recall archive
121 recalls · page 1 of 6
Reported Sep 23, 2026
Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
Matched: Brand · Product · Product details — The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions,…
7 more products in this recall
FDA (weekly enforcement report)
Reported Sep 9, 2026Updated Sep 14, 2026
Medline Convenience Kits: 1) CDS840396X, Catalog Number: CDS840396X; 2) CDS840396Y, Catalog Number: CDS840396Y; 3)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to…
28 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
American Contract System Convenience Kit, D & C PACK, Model/Catalog Number: LLPD90H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems Inc.
Matched: Reason for recall — The Convenience Kits contain Medline's Red Rubber Intermittent Catheters (8Fr-22 Fr) and Red Rubber Intermittent Catheter Trays. Medline Industries,…
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Medline breathing circuits labeled as: 1) MEDLINE HUDSON RCI, CIRCUIT, NEO, SING LIMB, HTD,COLUMN, Medline Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit…
18 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
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 Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concentration to levels below specification prior to the end of…
3 more products in this recall
FDA (openFDA device enforcement)
Medical devicesReported Aug 6, 2026Updated Sep 17, 2026
Medline Industries, LP recalls Medline, Teleflex Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits due to Due to heated wire connector (pigtail) at the…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Medline Industries, LP
Matched: Brand · Product · Product details — Due to heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized…
FDA (recalls & safety alerts)
Reported Jul 29, 2026
MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G
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 is issuing a recall for specific Medline kits containing B. Braun convenience kits that include Bupivacaine Hydrochloride in…
17 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 22, 2026
Medline Kits containing Zimmer Biomet mixing bowls and spatulas TOTAL KNEE PACK DYNJT6267
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Kits contain Zimmer Biomet mixing bowls and spatulas, which were recalled due to seal nonconformities which present risk of sterility breach. Health…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Medline Remedy Specialized Silicone Cream (Hydraguard-D ),Manufactured for Medline Industries, LP, Three Lakes Drive,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMed Laboratories, LLC.
Matched: Product · Product details — Failed Impurities/Degradation Specifications; Formaldehyde levels exceeded specification.
FDA (openFDA drug enforcement)
Reported Jul 15, 2026
Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots…
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE, Model Number: ART1145; 2) Universal Central/Art Line…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd.…
23 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Medline Convenience Kits: 1) DYNJ905503F, Model Number: CV ANESTHESIA - ROOM SET UP; 2) DYNJ905503G, Model Number: CV…
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 — The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in…
19 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Medline EBSI Kit EBSI1534
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable…
63 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 3, 2026
Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline…
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 kits were distributed containing Huons Bupivacaine Hydrochloride in Dextrose Injection, USP, which was subsequently recalled due to quality…
7 more products in this recall
FDA (openFDA device enforcement)
Reported May 20, 2026
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock,…
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 has identified the presence of particulate within the fluid path of the Manifolds.
10 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
Medline Convenience Kits: 1) ANCILLARY PACK-LF, Model Number:DYNJ0185290G; 2) OPEN HEART ANESTHESIA ICC-A, Model…
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 issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the…
41 more products in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
Medline Neuro Sponges, various dimensions, labeled as: 1. Neuro Sponges, Eponges neuro, Neuroesponjas, size 0.25" X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details · Reason for recall — During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that…
37 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Medline Namic Guidewires: 1) GUIDEWIRE 3MMJ 0.035X260CM LT, Model Number: DYNJGWIRE20L; 2) GWIRE HYDRO 0.035 180CM ANG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
38 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
FDA (openFDA device enforcement)
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)
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)
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)
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)
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)
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