Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy

Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Medline Medical Convenience Kits Recalled for Compromised Sterile Packaging

Agency Publication Date: February 9, 2026
Share:
Sign in to monitor this recall

Summary

Medline Industries, LP is recalling 54,301 medical convenience kits containing BD ChloraPrep Triple Swabsticks. These kits were distributed nationwide and include various sets for anesthesia, catheter dressing, dialysis, and surgical procedures. The recall was initiated because the swabstick applicators inside the kits may have open seals on their individual packaging, which can compromise the sterility of the medical device.

Risk

An open seal on the swabstick packaging could allow the sterile applicators to become contaminated. Using a non-sterile device during medical procedures increases the risk of serious infections for patients.

What You Should Do

  1. Check your medical supplies for various Medline medical convenience kits, including Anesthesia, Catheter Securement, Dialysis, Port Access, and Umbilical kits.
  2. Identify affected kits by checking the SKU, Lot Number, and UDI/DI on the product label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled products immediately to prevent potential patient infection.
  4. Contact Medline Industries, LP or your medical supply distributor to arrange for the return, replacement, or correction of the affected kits.
  5. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional information.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: ANESTHESIA ARTLINE PACK
Model / REF:
DYNJ47387B
Lot Numbers:
25EBJ414
UDI:
10193489217070

Recall #: Z-1326-2026; Quantity: 120 kits

Product: ADULT CATH SECUREMENT DRSG
Model / REF:
DYNDC3109
Lot Numbers:
25EBD613
UDI:
10193489918113

Recall #: Z-1327-2026; Quantity: 1350 kits

Product: PEDIATRIC CATH SECUREMENT DRSG
Model / REF:
DYNDC3108
Lot Numbers:
25EBD612
UDI:
10193489918007

Recall #: Z-1328-2026; Quantity: 450 kits

Product: CANCER SERVICE PORT KIT
Model / REF:
DT22710
Lot Numbers:
25EBC812

Part of Recall #: Z-1329-2026

Product: LINE KIT
Model / REF:
DYNDA1857A
Lot Numbers:
25FBH991

Part of Recall #: Z-1329-2026

Product: PICC REMOVAL KIT
Model / REF:
DYNDC1978A
Lot Numbers:
25EBC577

Part of Recall #: Z-1329-2026

Product: PORT ACCESS TRAY
Model / REF:
DYNDC2367
Lot Numbers:
25EBS434

Part of Recall #: Z-1329-2026

Product: NICU CENTRAL LINE TRAY
Model / REF:
DYNDC2407B
Lot Numbers:
25FMG170

Part of Recall #: Z-1329-2026

Product: CVC DRESSING CHANGE W/ TEG CHG
Model / REF:
DYNDC3222A
Lot Numbers:
25EBK184

Part of Recall #: Z-1329-2026

Product: PICC PROCEDURE PACK
Model / REF:
DYNJ59067A
PHS950205004B
Lot Numbers:
25EBM461
25EBD386
25FMD059

Part of Recall #: Z-1329-2026

Product: UNIVERSAL KIT
Model / REF:
DT22010B
Lot Numbers:
25EBC888
UDI:
10653160351092

Part of Recall #: Z-1330-2026

Product: VAD ACCESS KIT
Model / REF:
DT22790C
Lot Numbers:
25EBO566
25EBD964
UDI:
10653160996965

Part of Recall #: Z-1330-2026

Product: PROCEDURE TRAY
Model / REF:
DYNDA2966A
Lot Numbers:
25EBN178
25EBL624
UDI:
10198459005848

Part of Recall #: Z-1330-2026

Product: PEDIATRIC CENTRAL LINE SMALL
Model / REF:
DYNDC2208C
Lot Numbers:
25EBC706
UDI:
10889942815333

Part of Recall #: Z-1330-2026

Product: PORT DRESSING KIT
Model / REF:
DYNDC3107
Lot Numbers:
25EBN742
UDI:
10193489917628

Part of Recall #: Z-1330-2026

Product: NON STERILE DIALYSIS KIT
Model / REF:
DYNDH1029C
Lot Numbers:
25EBC778
UDI:
10889942816453

Part of Recall #: Z-1330-2026

Product: UMBILICAL TRAY W/3.5&5FR CATH
Model / REF:
UVT1250
Lot Numbers:
25EBO757
UDI:
10653160995340

Part of Recall #: Z-1330-2026

Product: UMBILICAL VESSEL TRAY
Model / REF:
UVT835
Lot Numbers:
25FMI300
UDI:
10653160289180

Part of Recall #: Z-1330-2026

Product: HEMODIALYSIS TRAY
Model / REF:
VAR101HVAA
Lot Numbers:
25EBE079
UDI:
10193489388145

Part of Recall #: Z-1330-2026

Product: POWERGLIDE DRESSING CHANGE KIT
Model / REF:
DYNDH1576
Lot Numbers:
25EBP737
UDI:
10193489437041

Part of Recall #: Z-1331-2026

Product: CENTRAL LINE TRAY W/ CHLRP SWB
Model / REF:
RWM-DC57KC
Lot Numbers:
25EBE082
UDI:
10889942582013

Part of Recall #: Z-1331-2026

Product: SUTURE REMOVAL TRAY
Model / REF:
DYNDR1277A
Lot Numbers:
25EBO576
UDI:
10195327379308

Recall #: Z-1332-2026

Product: BLOOD CULTURE KIT NS
Model / REF:
DYNDH2088
Lot Numbers:
25EBU508
25EBE330
UDI:
10198459230363

Recall #: Z-1333-2026

Product: LVAD DRESSING CHANGE TRAY
Model / REF:
DM320C
Lot Numbers:
25EBQ881
UDI:
10653160997504

Part of Recall #: Z-1334-2026

Product: PORT AND IO ACCESS DRESSING KI
Model / REF:
DT15780A
Lot Numbers:
25EBH827
UDI:
10653160323303

Part of Recall #: Z-1334-2026

Product: PORT-A-CATH DRESSING CHANGE TR
Model / REF:
DT16615
Lot Numbers:
25EBC730
UDI:
10653160259268

Part of Recall #: Z-1334-2026

Product: LARGE BORE CENTRAL LINE DRSG C
Model / REF:
DT19660
Lot Numbers:
25EBD629
UDI:
10653160283041

Part of Recall #: Z-1334-2026

Product: CENTRAL LINE DRESSING CHANGE K
Model / REF:
DT19665
Lot Numbers:
25EBU086
UDI:
10653160283263

Part of Recall #: Z-1334-2026

Product: NEONATAL DRESSING CHANGE KIT
Model / REF:
DT21495
Lot Numbers:
25EMJ081
UDI:
10653160320593

Part of Recall #: Z-1334-2026

Product: NICU CVC DRESSING CHANGE TRAY
Model / REF:
DT22510A
Lot Numbers:
25EMJ351
UDI:
10193489499247

Part of Recall #: Z-1334-2026

Product: DRESSING CHANGE TRAY W/TEG CHG
Model / REF:
DYNDC3114B
Lot Numbers:
25EBI085
UDI:
10198459078880

Part of Recall #: Z-1334-2026

Product: DRESSING CHANGE KIT
Model / REF:
DYNDC3351
Lot Numbers:
25EBM451
UDI:
10195327475482

Part of Recall #: Z-1334-2026

Product: STERILE RESUTURE PACK
Model / REF:
DYNDL1980A
Lot Numbers:
25EBJ785
UDI:
10195327379292

Recall #: Z-1335-2026

Product: MERCY CIRCUMCISION TRAY
Model / REF:
CIT6135B
Lot Numbers:
25EBC648
UDI:
10653160990666

Recall #: Z-1336-2026

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98284
Status: Active
Manufacturer: Medline Industries, LP
Sold By: Hospital supply distributors; Direct medical sales
Manufactured In: United States
Units Affected: 11 products (120 kits; 1350 kits; 450 kits; 7570 kits; 21854 units; 7380 kits; 2448 kits; 4300 kits; 8445 kits; 216 kits; 168 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.