Reported Oct 21, 2026 · Ongoing · Updated Oct 26, 2026
Medline surgical convenience kits labeled as
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
155 of 155 products
| Model / number | Barcodes | Product as published |
|---|---|---|
DYNJ0826732J | 1019845900876440198459008765 | Medline product number/ , UDI/DI 10198459008764 (each) 40198459008765 (case), Lot Number 26BMB707 |
DYNJ0665837G | 1019845954368540198459543686 | Medline product number/ , UDI/DI 10198459543685 (each) 40198459543686 (case), Lot Number 26BBG404 |
DYNJ900454C | 1019348985710840193489857109 | Medline product number/ , UDI/DI 10193489857108 (each) 40193489857109 (case), Lot Number 26AMI490 |
DYNJ68420D | 1019532734171840195327341719 | Medline product number/ , UDI/DI 10195327341718 (each) 40195327341719 (case), Lot Number 26ABM059 |
DYNJ0665837G | 1019845954368540198459543686 | Medline product number/ , UDI/DI 10198459543685 (each) 40198459543686 (case), Lot Number 26ABC613 |
DYNJ905692J | 1019845929847940198459298470 | Medline product number/ , UDI/DI 10198459298479 (each) 40198459298470 (case), Lot Number 25LDB280 |
DYNJ908620D | 1019845943440240198459434403 | Medline product number/ , UDI/DI 10198459434402 (each) 40198459434403 (case), Lot Number 25LBA755 |
DYNJ900454C | 1019348985710840193489857109 | Medline product number/ , UDI/DI 10193489857108 (each) 40193489857109 (case), Lot Number 25KMJ136 |
DYNJ68420D | 1019532734171840195327341719 | Medline product number/ , UDI/DI 10195327341718 (each) 40195327341719 (case), Lot Number 25KBH758 |
DYNJ0826732J | 1019845900876440198459008765 | Medline product number/ , UDI/DI 10198459008764 (each) 40198459008765 (case), Lot Number 25JMK339 |
DYNJ905692J | 1019845929847940198459298470 | Medline product number/ , UDI/DI 10198459298479 (each) 40198459298470 (case), Lot Number 25JDB137 |
DYNJ908620D | 1019845943440240198459434403 | Medline product number/ , UDI/DI 10198459434402 (each) 40198459434403 (case), Lot Number 25JBW131 |
DYNJ900454C | 1019348985710840193489857109 | Medline product number/ , UDI/DI 10193489857108 (each) 40193489857109 (case), Lot Number 25IMF439 |
DYNJ908620D | 1019845943440240198459434403 | Medline product number/ , UDI/DI 10198459434402 (each) 40198459434403 (case), Lot Number 25IBO322 |
DYNJ60973A | 1019845903794840198459037949 | Medline product number/ , UDI/DI 10198459037948 (each) 40198459037949 (case), Lot Number 25IBE177 |
DYNJ0826732J | 1019845900876440198459008765 | Medline product number/ , UDI/DI 10198459008764 (each) 40198459008765 (case), Lot Number 25HME176 |
DYNJ80861F | 1019845939838440198459398385 | Medline product number/ , UDI/DI 10198459398384 (each) 40198459398385 (case), Lot Number 25HBP381 |
DYNJ908620D | 1019845943440240198459434403 | Medline product number/ , UDI/DI 10198459434402 (each) 40198459434403 (case), Lot Number 25HBL650 |
DYNJ0160348B | 1088994221159340889942211594 | Medline product number/ , UDI/DI 10889942211593 (each) 40889942211594 (case), Lot Number 25GDB473 |
DYNJ905692J | 1019845929847940198459298470 | Medline product number/ , UDI/DI 10198459298479 (each) 40198459298470 (case), Lot Number 25GDA168 |
- Amount recalled
- 8374 kits
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
Why it was recalled
Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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