Recall archive
126 recalls · page 1 of 6
Reported Oct 28, 2026Updated Nov 2, 2026
MEDLINE DRAPE C-SEC FEN CLEAR SCRN WIRE, Medline Product Number/SKU DYNJP6106
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 21, 2026Updated Oct 26, 2026
1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV SHUNT PACK-MARYVIEW, Medline…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may…
10 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 14, 2026Updated Nov 2, 2026
Rollator, Bariatric, Basic Steel, Burgundy, mechanical walker with four legs and a metal frame intended for medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand — The front fork stem bolt/wheel assembly may disconnect from the rollator frame tubing. If the front fork stem bolt/wheel assembly disconnects from…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 7, 2026Updated Oct 13, 2026
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medline Industries, LP
Matched: Brand · Product · Product details — Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat,…
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2026Updated Oct 8, 2026
Medline convenience kits containing Healthmark Instrument Channel Brushes. SINUS PACK DYNJ48258D and Sinus Pack…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries, LP
Matched: Brand · Product · Product details — Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacturer due to the potential for a sharp edge/burr on the end of…
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2026Updated Oct 8, 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,…
10 more products in this recall
FDA (openFDA device enforcement)
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 27, 2026
American Contract System Convenience Kit, CV B PACK, Model/Catalog Number: TNCB10AM
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 26, 2026
Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU…
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)
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