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FDA (Device enforcement)Recalled 2026-08-10class ii

Medline Industries, LP: Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3) CRANIOTOMY PACK-LF, Catalog Number: D

Is my product affected?

Medline Convenience Kits: 1) ANTERIOR SPINE PACK, Catalog Number: DYNJT10197; 2) CRANIOTOMY #IMF 56646-LF, Catalog Number: DYNJVB91001; 3) CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348O; 4) SLUH CRANIOTOMY PACK-LF, Catalog Number: DYNJ0369348P; 5) LAMINECTOMY PACK-LF, Catalog Number: DYNJ04342M; 6

  • UPC 10198459778865
  • UPC 40198459778866
  • UPC 10193489801170
  • UPC 40193489801171
  • UPC 10195327025892
  • UPC 40195327025893
  • UPC 10195327295417
  • UPC 40195327295418
  • UPC 10193489914672
  • UPC 40193489914673
  • UPC 10195327421977
  • UPC 40195327421978
  • UPC 10195327237011
  • UPC 40195327237012
  • UPC 10193489853230
  • UPC 40193489853231
  • UPC 10889942278909
  • UPC 40889942278900
  • UPC 10195327346119
  • UPC 40195327346110
  • UPC 10195327054502
  • UPC 40195327054503
  • UPC 10193489460254
  • UPC 40193489460255
  • UPC 10889942779437
  • UPC 40889942779438
  • UPC 10195327225209
  • UPC 40195327225200
  • UPC 10195327021238
  • UPC 40195327021239
  • UPC 10195327343156
  • UPC 40195327343157
  • UPC 10195327471606
  • UPC 40195327471607
  • UPC 10195327184056
  • UPC 40195327184057
  • UPC 10195327231316
  • UPC 40195327231317
  • UPC 10198459569524
  • UPC 40198459569525

Check against the official notice below — it lists the full affected range.

Hazard

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.

Details from the source

Reason for recall: 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. Distribution: US Nationwide. Quantity: 4013 kits Lot/code info: 1) DYNJT10197, UDI-DI: 10198459778865(each), 40198459778866(case), Lot Number: 26GBA998; 2) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case), Lot Number: 23HLA649; 3) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case), Lot Number: 23GLA935; 4) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case), Lot Number: 23GLA081; 5) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case), Lot Number: 23CLA457; 6) DYNJVB91001, UDI-DI: 10193489801170(each), 40193489801171(case), Lot Number: 23BLA516; 7) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case), Lot Number: 22IBO169; 8) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case), Lot Number: 22GBD964; 9) DYNJ0369348O, UDI-DI: 10195327025892(each), 40195327025893(case), Lot Number: 22DBU156; 10) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24KBH955; 11) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24JBB595; 12) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24GMF624; 13) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24CMJ263; 14) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24BMK244; 15) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 24AMF230; 16) DYNJ0369348P, UDI-DI: 10195327295417(each), 40195327295418(case), Lot Number: 23JBJ151; 17) DYNJ0369348P, UDI-DI: 10195327295417(eac

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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