Reported Sep 30, 2026 · Ongoing · Updated Oct 6, 2026
Medline Convenience Kits
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?
Medline Convenience Kits
5 of 5 products
| Model / number | Product as published |
|---|---|
DYNJ02516G | PEDS SINUS PACK |
DYNJ0342705J | SINUS PACK-LF |
DYNJ40094G | NASAL-LF |
DYNJ50699F | ENT PACK |
DYNJ83219 | EENT PACK |
- Lot codes and dates
15 of 15 products
Products covered by this recall # Barcodes Product as published 1 1019348951400140193489514002Lot Number: 22HME611; 2) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 2 1019348951400140193489514002Lot Number: 23GMI728; 3) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 3 1019348951400140193489514002Lot Number: 23EME909; 4) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 4 1019348951400140193489514002Lot Number: 23CMG752; 5) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 5 1019348951400140193489514002Lot Number: 23CMB449; 6) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 6 1019348951400140193489514002Lot Number: 23AMI951; 7) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 7 1019348951400140193489514002Lot Number: 22KMD941; 8) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 8 1019348951400140193489514002Lot Number: 22JMC071; 9) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case) 9 1019532717081340195327170814Lot Number: 22FMD388; 10) DYNJ40094G, UDI-DI: 10195327170813(each), 40195327170814(case) 10 1019348982655540193489826556Lot Number: 23HMA901; 11) DYNJ50699F, UDI-DI: 10193489826555(each), 40193489826556(case) 11 1019532724772040195327247721Lot Number: 23HMA420; 12) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case) 12 1019532724772040195327247721Lot Number: 23GBH079; 13) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case) 13 1019532724772040195327247721Lot Number: 23FBB663; 14) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case) 14 1019532724772040195327247721Lot Number: 23DBS195; 15) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case) 15 Lot Number: 22LBG199 - Amount recalled
- 695 kits
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may present health risks that could require medical intervention, such as neurovascular adverse events, febrile response, and/or local transient inflammation, hypotension, or nausea.
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.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.