Class II FDA device recall · Z-1597-2025

Class II — the FDA judged the product may cause temporary or medically reversible harm, with a remote chance of serious harm.

This is the FDA's risk judgment for this recall. It describes the potential of the product as a category — it does not establish that any specific unit harmed anyone. Most recalls are Class II or III.

Medline Convenience kits used for various procedures: 1) T A PACK, Model Number: DYNJ67791A; 2) NASAL PACK, Model Number: DYNJ66514; 3) ENT PACK, Model Number: DYNJ67775A; 4) T/A ENDO PACK, Model Number: DYNJ83158; 5) T & A PACK, Model Number: DYNJ0634878I; 6) PPM-ICD PACK-LF, Model Number: DYNJ15949D; 7) TONSIL PACK, Model Number: DYNJ44525C; 8) ENT TRAY, Model Number: DYNJ44391K; 9) ENT PACK, Model Number: DYNJ49300D; 10) NASAL PACK, Model Number: DYNJ61555B; 11) HEAD AND NECK, Model Number: DYNJ57287A; 12) SINUS ENDOSCOPY-LF, Model Number: DYNJ36720F; 13) ENT PACK, Model Number: DYNJ54035B; 14) ENT PACK, Model Number: DYNJ36516; 15) FESS PACK, Model Number: DYNJ59502B; 16) T AND A PACK, Model Number: DYNJ80790; 17) PK,ENT, Model Number: DYNJ57583; 18) ENT/LAP PACK, Model Number: DYNJ84876; 19) TONSIL PACK, Model Number: DYNJ50109B; 20) TONSIL, Model Number: DYNJ908452C; 21) CSS SINUS PACK, Model Number: DYNJ17005I; 22) ENT, Model Number: DYNJ910514; 23) ADULT ENT - OAKBEND, Model Number: DYNJ905762; 24) EENT SPLIT PACK-LF, Model Number: LLSCAENT01; 25) ENT PACK, Model Number: DYNJ31453D; 26) ENT PACK, Model Number: DYNJ59447A; 27) TONSIL PACK, Model Number: DYNJ26441R; 28) ORAL ENT PACK, Model Number: DYNJ58408A; 29) ENT PACK, Model Number: DYNJ51085; 30) DR LANO NASAL CHRISTUS, Model Number: DYNJ61196A; 31) ENT PACK, Model Number: DYNJ66178D; 32) BWNBORO EENT PACK-LF, Model Number: DYNJ37551A; 33) HEAD AND NECK PACK, Model Number: DYNJ68872F; 34) EENT PACK, Model Number: DYNJ50301C; 35) ENT PACK, Model Number: DYNJ40498B; 36) SHN-C-THYROIDECTOMY-LF, Model Number: DYNJ46869A; 37) MINOR CYSTO PACK, Model Number: DYNJ58727D; 38) TONSILS AND ADENOIDS, Model Number: DYNJ45171C; 39) T&A PACK, Model Number: DYNJ56543J; 40) ENT PACK, Model Number: DYNJ54035B; 41) TONSIL PACK, Model Number: DYNJ50109B; 42) ENT PACK, Model Number: DYNJ40139D; 43) NASAL/SEPTO PACK, Model Number: DYNJ32099A; 44) EENT SPLIT PACK-LF, Model Number: LLSCAENT01; 45) ENT PACK, Model Number: DYNJ53573A; 46) CHS ENT PACK II, Model Number: DYNJCH908; 47) SIMPLE NECK DISSECTION, Model Number: DYNJ47481F; 48) TONSIL PACK, Model Number: DYNJ81479A; 49) E.N.T. TRAY, Model Number: DYNJ22357K; 50) NASAL PACK, Model Number: DYNJ39317B; 51) HEAD AND NECK PACK, Model Number: DYNJ54321D; 52) T A PACK, Model Number: DYNJ67791A; 53) ENT PACK, Model Number: DYNJ42451B; 54) HEAD AND NECK PACK-FOX, Model Number: DYNJ53348C; 55) HEAD AND NECK PACK, Model Number: DYNJ58596B; 56) SINUS PACK, Model Number: DYNJ56262; 57) ENT PACK, Model Number: DYNJ51085; 58) TONSIL T AND A PACK SHD, Model Number: DYNJ68417C; 59) ENT PACK, Model Number: DYNJ48595; 60) T AND A PACK-LF, Model Number: DYNJ52611; 61) HEAD AND NECK PACK, Model Number: DYNJ81897B; 62) ENSEMBLE ORL THYROIDE-LF, Model Number: DYNJ43390A; 63) EENT PACK-LF, Model Number: DYNJ34728D; 64) ENT, Model Number: DYNJ910514; 65) TONSIL ADENOID CKHA-LF, Model Number: DYNJ41771C; 66) ENT PACK, Model Number: DYNJ68679B; 67) PACK,T & A ASC, Model Number: DYNJ906914; 68) EENT SPLIT PACK-LF, Model Number: LLSCAENT01; 69) ENT PACK, Model Number: DYNJ83603; 70) ENT PACK, Model Number: DYNJ32247; 71) PPM-ICD PACK-LF, Model Number: DYNJ15949D; 72) ENT PACK, Model Number: DYNJ31453D; 73) SINOSCOPY PACK-LF, Model Number: DYNJ25600L; 74) T & A PACK, Model Number: DYNJ38978C; 75) CSC-N T&A, Model Number: DYNJ50870D; 76) ENT I-LF, Model Number: DYNJS0702; 77) ENT KIT, Model Number: DYNJ902836F; 78) ENT PACK, Model Number: DYNJ66039B; 79) TONSIL CDS, Model Number: DYNJ907844D; 80) PACK,T & A ASC, Model Number: DYNJ906914

Why it was recalled

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Is your unit affected?

The recall covers only the specific lots or serial numbers the FDA listed. Enter the lot or serial number from your product's label and we'll check it against that list.

A match means your unit may be covered — stop and call your pharmacist before doing anything. No match suggests it isn't covered, but confirm anyway: code formats vary and lists can be incomplete. Your unit not being listed does not guarantee it is safe, and being listed does not mean you have been harmed.

Show the FDA's listed lot / code information

1) DYNJ67791A, UDI-DI: 10193489941715(each), 40193489941716(case), Lot Number: 24IBE758; 2) DYNJ66514, UDI-DI: 10193489359282(each), 40193489359283(case), Lot Number: 24IBE817; 3) DYNJ67775A, UDI-DI: 10193489996258(each), 40193489996259(case), Lot Number: 24IBG346; 4) DYNJ83158, UDI-DI: 10195327236885(each), 40195327236886(case), Lot Number: 24IBG449; 5) DYNJ0634878I, UDI-DI: 10195327694500(each), 40195327694501(case), Lot Number: 24IBG548; 6) DYNJ15949D, UDI-DI: 10195327573805(each), 40195327573806(case), Lot Number: 24IBG570; 7) DYNJ44525C, UDI-DI: 10193489232042(each), 40193489232043(case), Lot Number: 24IBG608; 8) DYNJ44391K, UDI-DI: 10195327457648(each), 40195327457649(case), Lot Number: 24IBG848; 9) DYNJ49300D, UDI-DI: 10193489297287(each), 40193489297288(case), Lot Number: 24IBH734; 10) DYNJ61555B, UDI-DI: 10195327608101(each), 40195327608102(case), Lot Number: 24IBH769; 11) DYNJ57287A, UDI-DI: 10193489854152(each), 40193489854153(case), Lot Number: 24IBH959; 12) DYNJ36720F, UDI-DI: 10198459079306(each), 40198459079307(case), Lot Number: 24IBQ081; 13) DYNJ54035B, UDI-DI: 10195327680541(each), 40195327680542(case), Lot Number: 24IBQ933; 14) DYNJ36516, UDI-DI: 10884389544112(each), 40884389544113(case), Lot Number: 24IBR105; 15) DYNJ59502B, UDI-DI: 10193489372939(each), 40193489372930(case), Lot Number: 24IBR121; 16) DYNJ80790, UDI-DI: 10195327079482(each), 40195327079483(case), Lot Number: 24IBR337; 17) DYNJ57583, UDI-DI: 10889942755332(each), 40889942755333(case), Lot Number: 24IBR873; 18) DYNJ84876, UDI-DI: 10195327431778(each), 40195327431779(case), Lot Number: 24IBR895; 19) DYNJ50109B, UDI-DI: 10198459115776(each), 40198459115777(case), Lot Number: 24IBS352; 20) DYNJ908452C, UDI-DI: 10195327610937(each), 40195327610938(case), Lot Number: 24JBD799; 21) DYNJ17005I, UDI-DI: 10193489241860(each), 40193489241861(case), Lot Number: 24JBF130; 22) DYNJ910514, UDI-DI: 10198459021411(each), 40198459021412(case), Lot Number: 24JBK654; 23) DYNJ905762, UDI-DI: 10193489507966(each), 40193489507967(case), Lot Number: 24JBK682; 24) LLSCAENT01, UDI-DI: 10080196120802(each), 40080196120803(case), Lot Number: 24JBK897; 25) DYNJ31453D, UDI-DI: 10195327286224(each), 40195327286225(case), Lot Number: 24JBM367; 26) DYNJ59447A, UDI-DI: 10193489707663(each), 40193489707664(case), Lot Number: 24JBM926; 27) DYNJ26441R, UDI-DI: 10198459085888(each), 40198459085889(case), Lot Number: 24JBN335; 28) DYNJ58408A, UDI-DI: 10889942969029(each), 40889942969020(case), Lot Number: 24JBN611; 29) DYNJ51085, UDI-DI: 10889942117284(each), 40889942117285(case), Lot Number: 24JBN781; 30) DYNJ61196A, UDI-DI: 10195327604240(each), 40195327604241(case), Lot Number: 24JBN797; 31) DYNJ66178D, UDI-DI: 10198459100307(each), 40198459100308(case), Lot Number: 24JBN811; 32) DYNJ37551A, UDI-DI: 10888277585720(each), 40888277585721(case), Lot Number: 24JBT022; 33) DYNJ68872F, UDI-DI: 10198459079269(each), 40198459079260(case), Lot Number: 24JBT065; 34) DYNJ50301C, UDI-DI: 10198459052330(each), 40198459052331(case), Lot Number: 24JBT456; 35) DYNJ40498B, UDI-DI: 10193489806779(each), 40193489806770(case), Lot Number: 24JBV199; 36) DYNJ46869A, UDI-DI: 10198459069949(each), 40198459069940(case), Lot Number: 24JBV309; 37) DYNJ58727D, UDI-DI: 10198459048425(each), 40198459048426(case), Lot Number: 24JBV608; 38) DYNJ45171C, UDI-DI: 10889942485260(each), 40889942485261(case), Lot Number: 24JBV814; 39) DYNJ56543J, UDI-DI: 10195327453602(each), 40195327453603(case), Lot Number: 24JBW129; 40) DYNJ54035B, UDI-DI: 10195327680541(each), 40195327680542(case), Lot Number: 24JBW183; 41) DYNJ50109B, UDI-DI: 10198459115776(each), 40198459115777(case), Lot Number: 24JBW623; 42) DYNJ40139D, UDI-DI: 10195327663506(each), 40195327663507(case), Lot Number: 24JBX313; 43) DYNJ32099A, UDI-DI: 10195327610890(each), 40195327610891(case), Lot Number: 24JBY276; 44) LLSCAENT01, UDI-DI: 10080196120802(each), 40080196120803(case), Lot Number: 24JBY278; 45) DYNJ53573A, UDI-DI: 10193489201635(each), 40193489201636(case), Lot Number: 24JBY404; 46) DYNJCH908, UDI-DI: 10193489393347(each), 40193489393348(case), Lot Number: 24KBA907; 47) DYNJ47481F, UDI-DI: 10195327067335(each), 40195327067336(case), Lot Number: 24KBB421; 48) DYNJ81479A, UDI-DI: 10195327378370(each), 40195327378371(case), Lot Number: 24KBB455; 49) DYNJ22357K, UDI-DI: 10193489926736(each), 40193489926737(case), Lot Number: 24KBB793; 50) DYNJ39317B, UDI-DI: 10889942775729(each), 40889942775720(case), Lot Number: 24KBC590; 51) DYNJ54321D, UDI-DI: 10195327679323(each), 40195327679324(case), Lot Number: 24KBC663; 52) DYNJ67791A, UDI-DI: 10193489941715(each), 40193489941716(case), Lot Number: 24KBC754; 53) DYNJ42451B, UDI-DI: 10193489740318(each), 40193489740319(case), Lot Number: 24KBC910; 54) DYNJ53348C, UDI-DI: 10195327453565(each), 40195327453566(case), Lot Number: 24KBD155; 55) DYNJ58596B, UDI-DI: 10195327635947(each), 40195327635948(case), Lot Number: 24KBD243; 56) DYNJ56262, UDI-DI: 10889942624331(each), 40889942624332(case), Lot Number: 24KBD661; 57) DYNJ51085, UDI-DI: 10889942117284(each), 40889942117285(case), Lot Number: 24KBE334; 58) DYNJ68417C, UDI-DI: 10195327341633(each), 40195327341634(case), Lot Number: 24KBE396; 59) DYNJ48595, UDI-DI: 10888277915183(each), 40888277915184(case), Lot Number: 24KBE590; 60) DYNJ52611, UDI-DI: 10889942300853(each), 40889942300854(case), Lot Number: 24KBF355; 61) DYNJ81897B, UDI-DI: 10198459155710(each), 40198459155711(case), Lot Number: 24KBF577; 62) DYNJ43390A, UDI-DI: 10889942670321(each), 40889942670322(case), Lot Number: 24KBG019; 63) DYNJ34728D, UDI-DI: 10198459061851(each), 40198459061852(case), Lot Number: 24KBG035; 64) DYNJ910514, UDI-DI: 10198459021411(each), 40198459021412(case), Lot Number: 24KBG072; 65) DYNJ41771C, UDI-DI: 10889942599189(each), 40889942599180(case), Lot Number: 24KBG178; 66) DYNJ68679B, UDI-DI: 10195327129095(each), 40195327129096(case), Lot Number: 24KBG186; 67) DYNJ906914, UDI-DI: 10193489280173(each), 40193489280174(case), Lot Number: 24KBG371; 68) LLSCAENT01, UDI-DI: 10080196120802(each), 40080196120803(case), Lot Number: 24KBG399; 69) DYNJ83603, UDI-DI: 10195327284886(each), 40195327284887(case), Lot Number: 24KBG953; 70) DYNJ32247, UDI-DI: 10884389203873(each), 40884389203874(case), Lot Number: 24KBG965; 71) DYNJ15949D, UDI-DI: 10195327573805(each), 40195327573806(case), Lot Number: 24KBG993; 72) DYNJ31453D, UDI-DI: 10195327286224(each), 40195327286225(case), Lot Number: 24KBG996; 73) DYNJ25600L, UDI-DI: 10889942686247(each), 40889942686248(case), Lot Number: 24KBH226; 74) DYNJ38978C, UDI-DI: 10195327583590(each), 40195327583591(case), Lot Number: 24KBH242; 75) DYNJ50870D, UDI-DI: 10195327165666(each), 40195327165667(case), Lot Number: 24KBH280; 76) DYNJS0702, UDI-DI: 10080196798728(each), 40080196798729(case), Lot Number: 24KBI176; 77) DYNJ902836F, UDI-DI: 10198459002816(each), 40198459002817(case), Lot Number: 24KBI638; 78) DYNJ66039B, UDI-DI: 10195327151997(each), 40195327151998(case), Lot Number: 24KBL783; 79) DYNJ907844D, UDI-DI: 10195327387334(each), 40195327387335(case), Lot Number: 24KBP945; 80) DYNJ906914, UDI-DI: 10193489280173(each), 40193489280174(case), Lot Number: 24LBA080

Recall status

Ongoing — the recall is still being carried out.

Where it was distributed

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Recall record

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product type: Devices
Recall number: Z-1597-2025
Voluntary / mandated: Voluntary: Firm initiated
Initial notification: Letter
Origin: Northfield, IL
Recall initiated: 2025-03-03

What to do

Check the lot/code above against your product. To confirm this record and read the FDA's full notice, see the FDA recall page. Before changing anything you take or use, ask your pharmacist or prescriber — this page does not tell you to start or stop any drug or device.

Also available: structured data (JSON-LD) · recall record (JSON)

What this is — and is not

A recall is a recorded FDA enforcement action — the FDA logged that a firm is removing or correcting a product. It does not establish that any specific unit harmed anyone, and causation is not established by a recall. The class above is the FDA's risk judgment for the product category, not a finding about your unit. This page informs and compares; it is not medical advice and never tells you to start or stop a drug or device.

To report a problem you experienced, use FDA MedWatch. Verify this record at FDA recalls · Recall Z-1597-2025 · Source: openFDA enforcement.