Medline Industries, LP recalls Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU…
Kits contain a potentially contaminated component which were recalled by the manufacturer
Read the official notice →- Date
- 2026-09-02
- Country
- United States
- Brand
- Medline Industries
- Product
- Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU…
- Classification
- Class II
- Units
- US Nationwide distribution in the states of AL, CA, FL, IL, KS, LA, MA, MD,…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Medline Industries recalls
- 2026-09-23
USMedline Industries, LP recalls Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of…
- 2026-09-09
- US
Medline Industries, LP recalls Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE…
Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially…
- US
Medline Industries, LP recalls Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number:…
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 wrinkles in the paper lidding which may extend to the seal area. If the…
- 2026-09-02
- US
Medline Industries, LP recalls Medline medical convenience kit labeled as: TRACH TUBE KIT, Medline Kit SKU DYKM2330
Component labeling discrepancy
FDA · DeviceMedline Industries, LPUS Nationwide distribution in the state of California.Official notice → - US
Medline Industries, LP recalls Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3)…
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.
FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AZ, CA, IA, ID, IL, IN, MA, MD,…Official notice → - US
Medline Industries, LP recalls Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product…
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of…
FDA · DeviceMedline Industries, LPWorldwide distribution - US Nationwide and the country of Panama.Official notice →
Other drugs & medical recalls in the United States
- 2026-09-02
- US
IMRIS Imaging Inc recalls ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz…
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the…
FDA · DeviceIMRIS Imaging IncWorldwide distribution - US Nationwide and the countries of Canada, China,…Official notice → - US
Healthmark Industries Co., Inc. recalls healthmark ProChek-II, Model Number PT-313, PT-201-12
Test manufactured with an expired ingredient which may present as either a false negative or positive.
FDA · DeviceHealthmark Industries Co., Inc.Worldwide distribution - US Nationwide and the countries of Canada, France,…Official notice → - US
FUJIFILM Healthcare Americas Corporation recalls FUJIFILM Synapse PACS software v7.4.310; radiological image processing system
Software issue may cause the ruler measurement to be inaccurate.
FDA · DeviceFUJIFILM Healthcare Americas CorporationWorldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH,…Official notice → - US
ConMed Corporation recalls CONMED Linvatec GENESYS CrossFT Suture Anchor with Disposable Driver REF# CFBC-5502B 5.5mm GENESYs CrossFT Suture Anchor with two, #2 (5…
Suture anchor may contain incorrect patient implant card which may result in incorrect device identification and traceability.
- US
Fresenius Medical Care Renal Therapies Group, LLC recalls Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.
FDA · DeviceFresenius Medical Care Renal Therapies Group, LLCUS Nationwide distribution.Official notice → - US
Henry Schein Inc. recalls Structur 2 SC Temporary Resin Cartridge Refill 75Gm, Product Codes: 1) 114-3933, Mfr Product Code 1479; Lots 2536179, 2606429 2) 114-3934,…
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.
FDA · DeviceHenry Schein Inc.Worldwide distribution - US Nationwide and the country of Barbados.Official notice →