Medline PowerGlide Dressing Kits Recall: Open Seal Risk
Medline recalls specific medical kits with BD ChloraPrep Triple Swabsticks that may have open packaging seals. Affected kits include POWERGLIDE DRESSING CHANGE KIT SKU DYNDH1576 and CENTRAL LINE TRAY W/ CHLRP SWB SKU RWM-DC57KC. Stop using if you have these kits.
Use caution until it’s fixed
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
Contact the company
What happened, in plain English
Medline is recalling two specific medical convenience kits that contain BD ChloraPrep Triple Swabsticks with a potential open seal on the packaging. This could lead to contamination or improper use of the swabsticks if the seal is compromised. Read more at govinfonow.com/recall/50343-medline-powerglide-dressing-kits-recall-open-seal-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/50343-medline-powerglide-dressing-kits-recall-open-seal-risk · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1331-2026
Cite this page
“Medline PowerGlide Dressing Kits Recall: Open Seal Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/50343-medline-powerglide-dressing-kits-recall-open-seal-risk. Based on FDA recall #Z-1331-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1331-2026%22&limit=1).
Why it’s dangerous
The packaging of the BD ChloraPrep Triple Swabsticks may have an open seal, which could allow contamination or improper use of the swabsticks. This poses a risk if the seal is compromised during storage or handling.
Who’s affected
Healthcare workers and patients using Medline's POWERGLIDE DRESSING CHANGE KIT (SKU DYNDH1576) or CENTRAL LINE TRAY W/ CHLRP SWB (SKU RWM-DC57KC) from specific lots. Those handling medical supplies are most at risk.
How to tell if you have this one
Check for the kit SKU DYNDH1576 with lot number 25EBP737 or SKU RWM-DC57KC with lot number 25EBE082. These kits were sold with specific UDI/DI numbers.
- Brand
Medline- Category
Medical device
All 11 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class II- Status
Ongoing- Distribution
US Nationwide distribution.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-1326-2026 | Medline medical convenience kits packaged as: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B; UDI/DI 10193489217070, Lot Number 25EBJ414 | 120 kits |
| Z-1327-2026 | Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109; UDI/DI 10193489918113, Lot Number 25EBD613 | 1350 kits |
| Z-1328-2026 | Medline medical convenience kits packaged as: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108; UDI/DI 10193489918007, Lot Number 25EBD612 | 450 kits |
| Z-1329-2026 | Medline medical convenience kits packaged as: 1) CANCER SERVICE PORT KIT, Kit SKU DT22710; 2) LINE KIT, Kit SKU DYNDA1857A; 3) PICC REMOVAL KIT, Kit SKU DYNDC1978A; 4) PORT ACCESS TRAY, Kit SKU DYNDC2367; 5) NICU CENTRAL LINE TRAY, Kit SKU DYNDC2407B; 6) CVC DRESSING CHANGE W/ TEG CHG, Kit SKU DYNDC3222A; 7) PICC PROCEDURE PACK, Kit SKU DYNJ59067A; 8) PICC PROCEDURE PACK, Kit SKU PHS950205004B.; 1) Kit SKU DT22710, Lot Numbers: 25EBC812; 2) Kit SKU DYNDA1857A, Lot Numbers: 25FBH991; 3) Kit SKU DYNDC1978A, Lot Numbers: 25EBC577; 4) Kit SKU DYNDC2367, Lot Numbers: 25EBS434; 5) Kit SKU DYNDC2407B, Lot Numbers: 25FMG170; 6) Kit SKU DYNDC3222A, Lot Numbers: 25EBK184; 7) Kit SKU DYNJ59067A, Lot Numbers: 25EBM461, 25EBD386; 8) Kit SKU PHS950205004B, Lot Numbers: 25FMD059. | 7570 kits |
| Z-1330-2026 | 1) UNIVERSAL KIT, Kit SKU DT22010B; 2) VAD ACCESS KIT, Kit SKU DT22790C; 3) VAD ACCESS KIT, Kit SKU DT22790C; 4) PROCEDURE TRAY, Kit SKU DYNDA2966A; 5) PROCEDURE TRAY, Kit SKU DYNDA2966A; 6) PEDIATRIC CENTRAL LINE SMALL, Kit SKU DYNDC2208C; 7) PORT DRESSING KIT, Kit SKU DYNDC3107; 8) NON STERILE DIALYSIS KIT, Kit SKU DYNDH1029C; 9) UMBILICAL TRAY W/3.5&5FR CATH, Kit SKU UVT1250; 10) UMBILICAL VESSEL TRAY, Kit SKU UVT835; 11) HEMODIALYSIS TRAY, Kit SKU VAR101HVAA.; 1) Kit SKU DT22010B, UDI/DI 10653160351092, Lot number 25EBC888; 2) Kit SKU DT22790C, UDI/DI 10653160996965, Lot number 25EBO566; 3) Kit SKU DT22790C, UDI/DI 10653160996965, Lot number 25EBD964; 4) Kit SKU DYNDA2966A, UDI/DI 10198459005848, Lot number 25EBN178; 5) Kit SKU DYNDA2966A, UDI/DI 10198459005848, Lot number 25EBL624; 6) Kit SKU DYNDC2208C, UDI/DI 10889942815333, Lot number 25EBC706; 7) Kit SKU DYNDC3107, UDI/DI 10193489917628, Lot number 25EBN742; 8) Kit SKU DYNDH1029C, UDI/DI 10889942816453, Lot number 25EBC778; 9) Kit SKU UVT1250, UDI/DI 10653160995340, Lot number 25EBO757; 10) Kit SKU UVT835, UDI/DI 10653160289180, Lot number 25FMI300; 11) Kit SKU VAR101HVAA, UDI/DI 10193489388145, Lot number 25EBE079. | 21854 units |
| Z-1331-2026 | Medline medical convenience kits packaged as: 1) POWERGLIDE DRESSING CHANGE KIT, Kit SKU DYNDH1576; 2) CENTRAL LINE TRAY W/ CHLRP SWB, Kit SKU RWM-DC57KC.; 1) Kit SKU DYNDH1576, UDI/DI 10193489437041, Lot Number 25EBP737; 2) Kit SKU RWM-DC57KC, UDI/DI 10889942582013, Lot Number 25EBE082. | 7380 kits |
| Z-1332-2026 | Medline medical convenience kits packaged as: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A; UDI/DI 10195327379308, Lot Number 25EBO576 | 2448 kits |
| Z-1333-2026 | Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088; UDI/DI 10198459230363, Lot Numbers: 25EBU508, 25EBE330. | 4300 kits |
| Z-1334-2026 | Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESSING CHANGE K, Kit SKU DT19665; 6) NEONATAL DRESSING CHANGE KIT, Kit SKU DT21495; 7) NICU CVC DRESSING CHANGE TRAY, Kit SKU DT22510A; 8) DRESSING CHANGE TRAY W/TEG CHG, Kit SKU DYNDC3114B; 9) DRESSING CHANGE KIT, Kit SKU DYNDC3351.; 1) Kit SKU DM320C, UDI/DI 10653160997504, Lot Number 25EBQ881; 2) Kit SKU DT15780A, UDI/DI 10653160323303, Lot Number 25EBH827; 3) Kit SKU DT16615, UDI/DI 10653160259268, Lot Number 25EBC730; 4) Kit SKU DT19660, UDI/DI 10653160283041, Lot Number 25EBD629; 5) Kit SKU DT19665, UDI/DI 10653160283263, Lot Number 25EBU086; 6) Kit SKU DT21495, UDI/DI 10653160320593, Lot Number 25EMJ081; 7) Kit SKU DT22510A, UDI/DI 10193489499247, Lot Number 25EMJ351; 8) Kit SKU DYNDC3114B, UDI/DI 10198459078880, Lot Number 25EBI085; 9) Kit SKU DYNDC3351, UDI/DI 10195327475482, Lot Number 25EBM451. | 8445 kits |
| Z-1335-2026 | Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A; UDI/DI 10195327379292, Lot Number 25EBJ785 | 216 kits |
| Z-1336-2026 | Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B; UDI/DI 10653160990666, Lot Number 25EBC648 | 168 units |
What to do — step by step
Check Kit Details
Look for the specific SKU and lot number on the packaging to confirm if your kit is affected.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 56 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Do I need to stop using these kits immediately?
The recall does not require immediate stop use; however, you should check if your kit is affected and take action if it is.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-1331-2026 (December 24, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1331-2026 to see it in context.
- Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.