Centurion dialysis and dressing change kits contain recalled Mastisol adhesive
Centurion convenience kits including dialysis catheter maintenance and dressing change trays are being recalled because they contain a recalled lot of Mastisol Liquid Adhesive.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: FDA Class II recall where the described consequence is that a component becomes unusable rather than any patient hazard, which fits the Moderate band.
Plain-English summary
Centurion convenience kits are being recalled, covering the Central Line Dressing SV43 FCP (DYNDC2356B), the Dialysis Catheter Maintenance Kit (DT17570), the Dialysis Dressing Change Kit (DT21370B), the Dressing Change Tray - Gold (DT21115B) and the Port Dressing Change Kit, among the SKUs listed in the recall notice. The action covers 49,654 kits in total across the connected Mastisol recalls.
The stated reason is that the kits contain a recalled lot of Ferndale Laboratories Mastisol Liquid Adhesive. According to the notice, the butyrate tubing may crack during actuation and render the product unusable for application. The FDA classified the action as Class II. The source does not describe any patient hazard beyond the product being unusable.
Distribution was nationwide in the United States, with distribution outside the United States pending.
Facilities should identify affected stock using the kit numbers, UDI-DI codes and lot numbers in the recall notice and follow the instructions issued by the firm.
The recalled product
- Product
- Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570 DIALYSIS DRESSING CHANGE KIT DT21370B DRESSING CHANGE TRAY - GOLD DT21115B PORT DRESSING CHANGE KIT DYNDC2815A
- Manufacturer
- Medline Industries, LP
- Category
- Medical Device — Dressing kit
- Affected units
- 49,654
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 34 recalled by Medline Industries, LP under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 34 products in this recall →Related recalls
Same manufacturer · Medline Industries, LP
See all →- HighMedline C-Section Convenience Kits Recalled for Contaminated Components
FDA (Devices) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- HighMedline Recalls 419 Surgical Kits Due to Contaminated Component
FDA (Devices) · 2026-09-02
- HighMedline Recalls Neonatal Heated Wire Breathing Circuits Due to Thermal Damage
FDA (Devices) · 2026-09-02
- SevereMedline Neonatal Heated Wire Breathing Circuits Recalled for Thermal Failure
FDA (Devices) · 2026-09-02
Same hazard · component defect
See all →- ModerateMedline da Vinci main kits contain recalled Mastisol liquid adhesive
FDA (Devices) · 2026-06-24
- ModerateMedline femoral block trays contain recalled Mastisol liquid adhesive
FDA (Devices) · 2026-06-24
- ModerateMedline breast hernia port kits contain recalled Mastisol liquid adhesive
FDA (Devices) · 2026-06-24
- ModerateMedline EBSI dressing change kits contain recalled Mastisol liquid adhesive
FDA (Devices) · 2026-06-24
- ModerateMedline EBSI kits contain recalled Mastisol liquid adhesive
FDA (Devices) · 2026-06-24