Skip to content
Get alerts
GovInfoNow
Lower risk Medical device recall · FDA · Published March 19, 2025

Medline procedure kits with leaking bottles recalled: Risk of contamination

Medline recalls procedure kits (T AND A PACK -LF, REF DYNJ85792) due to leaking sterile water and saline bottles. Affected kits may cause contamination if used.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1707-2025Medical deviceMedline ›
Take action

Contact the company

Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer

Medline is recalling procedure kits labeled T AND A PACK -LF, REF DYNJ85792 because the sterile water and saline bottles leak at the bottle opening. This could lead to contamination if the kits are used. Read more at govinfonow.com/recall/52596-medline-procedure-kits-with-leaking-bottles-recalled-risk-of-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/52596-medline-procedure-kits-with-leaking-bottles-recalled-risk-of-contamination · Updated August 18, 2026 · FDA enforcement record: FDA #Z-1707-2025

Cite this page

“Medline procedure kits with leaking bottles recalled: Risk of contamination.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/52596-medline-procedure-kits-with-leaking-bottles-recalled-risk-of-contamination. Based on FDA recall #Z-1707-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1707-2025%22&limit=1).

The FDA announced on March 19, 2025, that Medline Industries LP of Northfield is recalling Medline procedure kits labeled as T AND A PACK -LF due to leaking sterile water and saline bottles. The agency issued recall number Z-1707-2025 for the Class II voluntary recall.

How to tell if you have it

  • Brand: Medline
  • Product: Medline procedure kits, labeled as T AND A PACK -LF
  • Reference: REF DYNJ85792
  • UDI/DI: 10195327552350 (EA) 40195327552351 (CS)
  • Lot Numbers: 24BBB747
  • Quantity: 30 units
  • Distribution: US Nationwide, Panama, and Canada

The hazard

According to the FDA, the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were identified as leaking at the interface of the peel-foil and bottle opening.

Context

GovInfoNow's records show MEDLINE INDUSTRIES, LP - Northfield has 119 other recalls on record since October 22, 2021. Other recent recalls of similar products include Medline medical kits recalled due to light failure in intubation trays (July 25, 2025), Medline Recalls Foley Tray Kits with Incorrect Labeling Risk (July 23, 2025), and Medline ReNewal Reprocessed St. Jude Catheters May Contain Particulates (July 14, 2025). Additional similar recalls include Medline Medical Kits Recalled Due to Cracked Adhesive Risk (December 12, 2025), Medline Convenience Kits Recall: Risk of Sterile Packaging Breach (June 12, 2026), and Medline Convenience Kits Recall: Contaminated Components Risk (July 10, 2026).

How to tell if you have this one

Check for the label 'T AND A PACK -LF, REF DYNJ85792' on the kit. The lot number 24BBB747 is also associated with this recall.

  • Brand
    Medline
  • Category
    Medical device
FDA recall event · 10 products

All 10 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
    Worldwide distribution - US Nationwide and the countries of Panama and Canada.
Recall numberProduct, codes & lotsQuantity
Z-1705-2025Medline Sterile Water, USP, 100mL, REF RDI30295; UDI/DI 10884389338230 (EA) 40884389338231 (CS), Lot Numbers: 23CJA159, 23GJA086, 23HJA080, 23JJA010, 23KJA047, 23LJA031, 23LJA089, 24AJA095, 24AJA157, 24CJA089, 24IJA004, 24IJA036, 24JJA164, 24KJA008, 24KJA051, 24KJA108.963054 units
Z-1706-2025Medline Sterile 0.9% Normal Saline, USP, 100mL, REF RDI30296; UDI/DI 10884389338247 (EA) 10884389338230 (CS), Lot Numbers: 23DJA038, 23DJA070, 23DJA114, 23EJA057, 23EJA128, 23EJA144, 23FJA110, 23GJA041, 23GJA118, 23GJA132, 23HJA033, 23IJA045, 23IJA052, 23IJA102, 23JJA103, 23JJA119, 23JJA144, 23LJA114, 24AJA025, 24AJA061, 24AJA180, 24BJA038, 24BJA092, 24BJA119, 24BJA158, 24CJA048, 24CJA117, 24CJA147, 24DJA010, 24HJA075, 24HJA178, 24KJA148.2519991 units
Z-1707-2025Medline procedure kits, labeled as: T AND A PACK -LF, REF DYNJ85792; UDI/DI 10195327552350 (EA) 40195327552351 (CS), Lot Numbers: 24BBB74730 units
Z-1708-2025Medline procedure kits, labeled as: NON STERILE I&D KIT, REF DYKM1438; UDI/DI 10889942529964 (EA) 40889942529965 (CS), Lot Numbers: 23KDB283240 units
Z-1709-2025Medline procedure kits, labeled as: 1) STERILE PREP KIT, REF DYNDA1359A; 2) STRL EK SINGLE PACK, REF DYNDA1360B; 3) SHEATH REMOVAL TRAY, REF DYNDC1311C; 4) SENSITIVE SKIN WEEKLY VAD, REF DYNDC3185; 5) NURSING SKILLS, REF EDUC05015A; 6) NURSING SUPPLY BAG, REF EDUC1024A.; 1) REF DYNDA1359A: UDI/DI 10195327417734 (EA) 40195327417735 (CS), Lot Numbers: 23KBW508; 2) REF DYNDA1360B: UDI/DI 10889942903863 (EA) 40889942903864 (CS), Lot Numbers: 23KBB406; 3) REF DYNDC1311C: UDI/DI 10080196151561 (EA) 40080196151562 (CS), Lot Numbers: 23KBX338; 4) REF DYNDC3185: UDI/DI 10195327034108 (EA) 40195327034109 (CS), Lot Numbers: 23KBX632; 5) REF EDUC05015A: UDI/DI 10193489849035 (EA) 40193489849036 (CS), Lot Numbers: 23LDA746, 23LDA814, 23LDA218; 6) REF EDUC1024A: UDI/DI 10195327493165 (EA) 40195327493166 (CS), Lot Numbers: 23LDA281, 23KDA001.822 units
Z-1710-2025Medline procedure kits, labeled as: PLASTICS SUTURE TRAY, REF SUT13535; UDI/DI 10653160144250 (EA) 40653160144251 (CS), Lot Numbers: 23JBU525120 units
Z-1711-2025Medline procedure kits, labeled as: 1) WOUND CARE TRAY, REF DYNDA1412A; 2) LACERATION TRAY, REF DYNDL1263A.; 1) REF DYNDA1412A: UDI/DI 10193489693423 (EA) 40193489693424 (CS), Lot Numbers: 23KBH040; 2) REF DYNDL1263A: UDI/DI 10884389347126 (EA) 40884389347127 (CS), Lot Numbers: 23KBD401.5200 units
Z-1712-2025Medline procedure kits, labeled as: REDDY JOINT BATH, REF MMJB001A; UDI/DI 10195327514877 (EA) 40195327514878 (CS), Lot Numbers: 24BBJ082, 23KBH046, 23JBD1372220 units
Z-1713-2025Medline procedure kits, labeled as: OL OCULAR, REF DYNJ906183K; UDI/DI 10195327385521 (EA)40195327385522 (CS), Lot Numbers: 23LME29930 units
Z-1714-2025Medline procedure kits, labeled as: HAND, REF DYNJ902002J; UDI/DI 10195327516079 (EA) 40195327516070 (CS), Lot Numbers: 24ABC106, 23KBN892, 23JBV265159 units
Based on the official FDA remedy

What to do — step by step

  1. Check Kit Label

    Look for the label 'T AND A PACK -LF, REF DYNJ85792' on the procedure kit.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Panama and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 49 days after the firm started it.

1. Firm started the recall: Mar 19, 202512. FDA classified it Class II: May 1, 202523. Published in FDA’s Enforcement Report: May 7, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

Safeguard US Recalls Battle Bandages and IFAK Kits Due to Infection Risk
Safeguard US Operating LLCMiniMed Flex Insulin Pump Recall: Inaccurate Delivery Risk
Medtronic MiniMed, Inc.Medline Bariatric Rollator Recall: Detaching Wheels Risk
Medline Industries, LPCooperVision Pearle Vision 1 Day Contact Lenses: Incorrect Power Risk
CooperVision, Inc.Tandem t:slim App Recall: Pairing Issue With Abbott Sensors
Tandem Diabetes Care, Inc.

Latest medical device recalls

BMC Medical Co., Ltd. recalls BMC/REACTHEALTH Luna G3 APAP REF LG 3600
BMC Medical Co., Ltd. · July 15, 2026Medtronic MiniMed, Inc. recalls MiniMed 670G Insulin Pump, Model: MMT-1781, MMT-1782;
Medtr: MiniMed · July 13, 2026INTEGRATED MEDCRAFT LLC recalls Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway
Medcraft · July 7, 2026Pride Mobility Products Corp. recalls Brand Name: Quantum Rehab Product Name: R-TRAK Model/Catalog Number: R-TRAK Software Version: 2.0.11, new version:
Quantum Rehab · June 25, 2026ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory
ResMed · June 25, 2026Therabody, Inc recalls Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
Therabody · June 23, 2026

Keep exploring

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-1707-2025 (March 19, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1707-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA