Lower riskMedical device recall · FDA · Published July 31, 2026
Medline Convenience Kits Risk Patient Infection Due to Sterile Packaging Issues
Medline recalls anesthesia pain kits with potential open seals in sterile pouches that could cause patient infections if used without proper sterility checks.
Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.
“Medline Convenience Kits Risk Patient Infection Due to Sterile Packaging Issues.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/1134646-medline-convenience-kits-risk-patient-infection-due-to-sterile-packaging. Based on FDA recall #Z-3207-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3207-2026%22&limit=1).
Medline Industries, LP voluntarily recalled Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A due to potential open seals in sterile pouch packaging that may compromise sterility, the FDA said on July 31, 2026. The recall affects 341 units distributed nationwide and in Arkansas, Florida, North Carolina, Maryland, and Texas.
How to tell if you have it
Brand: Medline
Product: Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A
UDI-DI: 10195327506506
Lot code: 25BBK494
The hazard
The kits may exhibit open seals in sterile pouch packaging, which may compromise product sterility. If not detected prior to use, the issue may lead to contamination of the sterile field or patient infection if the product is used.
Context
GovInfoNow's records show Medline Industries, LP has 68 other recalls on record since July 31, 2025. Other recent recalls include a Medline recall of Basic Homecare Beds and Medlite Homecare Beds on August 14, 2026, and a Medline Convenience Kits Recall for fungal contamination risk on August 11, 2026. Similar recent recalls of medical kits include Medical Action Industries Blood Culture Kits on July 23, 2026, Boston Scientific EndoVive Safety PEG Kit on February 10, 2026, and AVID Medical Halyard IV Start Kit on July 14, 2026.
How to tell if you have this one
Check for the model number DYNJ67925A on the kit. The kits were sold with UDI-DI 10195327506506 Lot 25BBK494.
Brand
Medline
Category
Medical device
FDA recall event · 4 products
All 4 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 in states of Arkansas, Florida, North Carolina, Maryland, and Texas.
Recall number
Product, codes & lots
Quantity
Z-3207-2026
Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A; UDI-DI 10195327506506 Lot 25BBK494
341
Z-3208-2026
Convenience kits MINOR PACK DYNJ58421A SPRINGHILL MINOR PACK DYNJ40734F; DYNJ58421A UDI-DI 10193489970487 Lot 25HBQ049 DYNJ40734F UDI-DI 10198459162084 Lots 25GBO299 25IBS607
459
Z-3209-2026
Convenience kits MYRINGOTOMY PACK-LF DYNJ59097A; UDI-DI 10198459046551 Lot 25FBU754
60
Z-3210-2026
Convenience kits CATARACT PACK DYNJ59881A; UDI-DI 10198459020612 Lot 25GBP246
336
Based on the official FDA remedy
What to do — step by step
Check Sterility Packaging
Inspect the sterile pouch for open seals before use to ensure product sterility.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 5 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Arkansas, Florida, Maryland, North Carolina, Texas.
Recall timeline
FDA published this recall 54 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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-3207-2026 (July 31, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3207-2026 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.