medical MODERATE Updated 2026-09-30

Medline Industries, LP recalls Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Numbe

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Recalled Product

Medline Convenience Kits: 1) PEDS SINUS PACK, Catalog Number: DYNJ02516G; 2) SINUS PACK-LF, Catalog Number: DYNJ0342705J; 3) NASAL-LF, Catalog Number: DYNJ40094G; 4) ENT PACK, Catalog Number: DYNJ50699F; 5) EENT PACK, Catalog Number: DYNJ83219

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: 1) DYNJ02516G, UDI-DI: 10889942295234(each), 40889942295235(case), Lot Number: 22HME611; 2) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 23GMI728; 3) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 23EME909; 4) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 23CMG752; 5) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 23CMB449; 6) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 23AMI951; 7) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 22KMD941; 8) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 22JMC071; 9) DYNJ0342705J, UDI-DI: 10193489514001(each), 40193489514002(case), Lot Number: 22FMD388; 10) DYNJ40094G, UDI-DI: 10195327170813(each), 40195327170814(case), Lot Number: 23HMA901; 11) DYNJ50699F, UDI-DI: 10193489826555(each), 40193489826556(case), Lot Number: 23HMA420; 12) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case), Lot Number: 23GBH079; 13) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case), Lot Number: 23FBB663; 14) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case), Lot Number: 23DBS195; 15) DYNJ83219, UDI-DI: 10195327247720(each), 40195327247721(case), Lot Number: 22LBG199

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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