FDA · Class I · September 23, 2026
Illustration: An FDA laboratory that tests medical devices – not the recalled product. Photo: U.S. Food and Drug Administration, public domain.
Medline Industries recall: Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more products
Medline Industries, LP is recalling Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more products – 12 kits; 489 kits; 447 kits; 10407 kits; 2718 kits; 1100 kits; 47848 kits. The U.S. Food and Drug Administration published the recall on September 23, 2026; it began on August 11, 2026. Distributed nationwide.
Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.
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| Product | Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET and 6 more products |
| Brand | Medline Industries |
| Company | Medline Industries, LP |
| Type | Medical devices |
| Classification | Class I |
| Recall date | August 11, 2026 |
| Published by FDA | September 23, 2026 |
| Quantity | 12 kits; 489 kits; 447 kits; 10407 kits; 2718 kits; 1100 kits; 47848 kits |
| Recall ID | 99669 |
As listed by FDA
Recalled products (7)
- Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET, Catalog Number: DYKMBNDL199A
- FDA recall number
- Z-3121-2026
- Codes, lots and dates
- 1) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBH109; 2) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBM182; 3) DYKMBNDL199A, UDI-DI: 10193489848540(each), 40193489848541(case), Lot Number: 24HBS365
- Quantity
- 12 kits
- Classification
- Class I
- Medline Convenience Kits: 1) OPEN HEART ADULT, Catalog Number: CDS840396Y; 2) FULL LINE ANEURYSM CDS, Catalog Number: CDS983672O; 3) NON STERILE CHEST TUBE REMOVAL, Catalog Number: DYNDA1080
- FDA recall number
- Z-3122-2026
- Codes, lots and dates
- 1) CDS840396Y, UDI-DI: 10195327574932(each), 40195327574933(case), Lot Number: 24FBJ654; 2) CDS983672O, UDI-DI: 10195327207625(each), 40195327207626(case), Lot Number: 24FBM444; 3) CDS983672O, UDI-DI: 10195327207625(each), 40195327207626(case), Lot Number: 24HBJ581; 4) DYNDA1080, UDI-DI: 10884389388679(each), 40884389388670(case), Lot Number: 24HBT102
- Quantity
- 489 kits
- Classification
- Class I
- Medline Convenience Kits: 1) PORT ACCESS KIT UNIV OF ALA, Catalog Number: DYKM1414; 2) ARTERIAL LINE ST JOES SYR PACK, Catalog Number: DYNJ38145F
- FDA recall number
- Z-3123-2026
- Codes, lots and dates
- 1) DYKM1414, UDI-DI: 10889942481293(each), 40889942481294(case), Lot Number: 24HBS933; 2) DYNJ38145F, UDI-DI: 10193489277173(each), 40193489277174(case), Lot Number: 24HBT600
- Quantity
- 447 kits
- Classification
- Class I
- Medline Convenience Kits: 1) ACC010308A, Catalog Number: ACC010308A; 2) ACC010374A, Catalog Number: ACC010374A; 3) ACC010679, Catalog Number: ACC010679; 4) ACC010726A, Catalog Number: ACC010726A; 5) DYNDB3061, Catalog Number: DYNDB3061; 6) DYNDH1245, Catalog Number: DYNDH1245; 7) DYNDH1362, Catalog Number: DYNDH1362
- FDA recall number
- Z-3124-2026
- Codes, lots and dates
- 1) ACC010308A, UDI-DI: 10889942424597(each), 40889942424598(case), Lot Number: 24HDA993; 2) ACC010308A, UDI-DI: 10889942424597(each), 40889942424598(case), Lot Number: 24IDB285; 3) ACC010308A, UDI-DI: 10889942424597(each), 40889942424598(case), Lot Number: 24JDA212; 4) ACC010374A, UDI-DI: 10193489893977(each), 40193489893978(case), Lot Number: 24IDB849; 5) ACC010679, UDI-DI: 10195327396268(each), 40195327396269(case), Lot Number: 24HDA071; 6) ACC010726A, UDI-DI: 10198459043666(each), 40198459043667(case), Lot Number: 24GDB143; 7) DYNDB3061, UDI-DI: 10889942143733(each), 40889942143734(case), Lot Number: 24HBS752; 8) DYNDH1245, UDI-DI: 10889942604722(each), 40889942604723(case), Lot Number: 24FMH385; 9) DYNDH1362, UDI-DI: 10888277797086(each), 40888277797087(case), Lot Number: 24HBQ828
- Quantity
- 10407 kits
- Classification
- Class I
- Medline Convenience Kits: 1) DYKM1000B, Catalog Number: DYKM1000B; 2) DYKM2187A, Catalog Number: DYKM2187A
- FDA recall number
- Z-3125-2026
- Codes, lots and dates
- 1) DYKM1000B, UDI-DI: 10889942508143(each), 40889942508144(case), Lot Number: 24GMD979; 2) DYKM2187A, UDI-DI: 10195327628826(each), 40195327628827(case), Lot Number: 24FBM840; 3) DYKM2187A, UDI-DI: 10195327628826(each), 40195327628827(case), Lot Number: 24HBK903
- Quantity
- 2718 kits
- Classification
- Class I
- Medline Convenience Kits: 1) DYNDH1193, Catalog Number: DYNDH1193; 2) DYNDH1487A, Catalog Number: DYNDH1487A
- FDA recall number
- Z-3126-2026
- Codes, lots and dates
- 1) DYNDH1193, UDI-DI: 10889942499953(each), 40889942499954(case), Lot Number: 24HBF076; 2) DYNDH1193, UDI-DI: 10889942499953(each), 40889942499954(case), Lot Number: 24HBU638; 3) DYNDH1487A, UDI-DI: 10193489484311(each), 40193489484312(case), Lot Number: 24FMH485
- Quantity
- 1100 kits
- Classification
- Class I
- Medline Convenience Kits: 1) DYNDB3086D, Catalog Number: DYNDB3086D; 2) DYNDB3100, Catalog Number: DYNDB3100; 3) DYNDH1619A, Catalog Number: DYNDH1619A; 4) DYNDH1620A, Catalog Number: DYNDH1620A; 5) DYNDH1694A, Catalog Number: DYNDH1694A; 6) DYNDH1695, Catalog Number: DYNDH1695; 7) DYNDH1708A, Catalog Number: DYNDH1708A; 8) DYNDH1714A, Catalog Number: DYNDH1714A; 9) DYNDH1723, Catalog Number: DYNDH1723; 10) DYNDH1740B, Catalog Number: DYNDH1740B; 11) DYNDH1741B, Catalog Number: DYNDH1741B; 12) DYNDH1771A, Catalog Number: DYNDH1771A; 13) DYNDH1908, Catalog Number: DYNDH1908; 14) DYNDH1940, Catalog Number: DYNDH1940; 15) DYNDH1988, Catalog Number: DYNDH1988; 16) DYNDH2002, Catalog Number: DYNDH2002; 17) DYNDH2017, Catalog Number: DYNDH2017. Blood and urine collection kits
- FDA recall number
- Z-3127-2026
- Codes, lots and dates
- 1) DYNDB3086D, UDI-DI: 10195327313234(each), 40195327313235(case), Lot Number: 24IBA685; 2) DYNDB3100, UDI-DI: 10198459028915(each), 40198459028916(case), Lot Number: 24IBF913; 3) DYNDH1619A, UDI-DI: 10195327215835(each), 40195327215836(case), Lot Number: 24FBH708; 4) DYNDH1619A, UDI-DI: 10195327215835(each), 40195327215836(case), Lot Number: 24HBG622; 5) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case), Lot Number: 24GBY827; 6) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case), Lot Number: 24HBQ593; 7) DYNDH1620A, UDI-DI: 10195327216047(each), 40195327216048(case), Lot Number: 24HBU881; 8) DYNDH1694A, UDI-DI: 10195327139957(each), 40195327139958(case), Lot Number: 24EBI901; 9) DYNDH1694A, UDI-DI: 10195327139957(each), 40195327139958(case), Lot Number: 24HBG834; 10) DYNDH1695, UDI-DI: 10195327113155(each), 40195327113156(case), Lot Number: 24FBQ907; 11) DYNDH1708A, UDI-DI: 10195327498368(each), 40195327498369(case), Lot Number: 24IBQ580; 12) DYNDH1714A, UDI-DI: 10195327347550(each), 40195327347551(case), Lot Number: 24EBI892; 13) DYNDH1714A, UDI-DI: 10195327347550(each), 40195327347551(case), Lot Number: 24IBE380; 14) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case), Lot Number: 24EBI893; 15) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case), Lot Number: 24GBH135; 16) DYNDH1723, UDI-DI: 10195327134204(each), 40195327134205(case), Lot Number: 24HBG826; 17) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case), Lot Number: 24EBV834; 18) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case), Lot Number: 24FBH710; 19) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case), Lot Number: 24FBK197; 20) DYNDH1740B, UDI-DI: 10198459006302(each), 40198459006303(case), Lot Number: 24GBW340; 21) DYNDH1741B, UDI-DI: 10198459006319(each), 40198459006310(case), Lot Number: 24FBJ622; 22) DYNDH1741B, UDI-DI: 10198459006319(each), 40198459006310(case), Lot Number: 24GBW330; 23) DYNDH1771A, UDI-DI: 10198459088971(each), 40198459088972(case), Lot Number: 24IBJ998; 24) DYNDH1908, UDI-DI: 10195327472467(each), 40195327472468(case), Lot Number: 24EBC055; 25) DYNDH1940, UDI-DI: 10195327526535(each), 40195327526536(case), Lot Number: 24FMH509; 26) DYNDH1988, UDI-DI: 10195327628772(each), 40195327628773(case), Lot Number: 24HBF080; 27) DYNDH2002, UDI-DI: 10195327689971(each), 40195327689972(case), Lot Number: 24GBO301; 28) DYNDH2002, UDI-DI: 10195327689971(each), 40195327689972(case), Lot Number: 24HBQ827; 29) DYNDH2017, UDI-DI: 10198459022159(each), 40198459022150(case), Lot Number: 24HBO219
- Quantity
- 47848 kits
- Classification
- Class I
Exactly as the agency lists them
Identifiers and details
- FDA event ID
- 99669
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Northfield, IL, United States
Why it was recalled
The reason the FDA lists: “The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99669, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Same brand
Other Medline Industries recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 |  Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Sep 30, 2026 | Medline Industries recall: Medline Convenience Kits: 1) PEDS SINUS PACK and 4 more productsMedical devices · 695 kits; 128 kits; 486 kits; 234 kits; 4013 kits | The kits contain neurological sponges with the potential for unexpected variability of end… Serious | FDA Class II |
| Sep 30, 2026 | Medline Industries recall: Medline convenience kits containing Healthmark Instrument Channel BrushesMedical devices · 90 kits (US) | Kits contain Healthmark Instrument Channel Brushes, which were recalled by the manufacture… Serious | FDA Class II |
| Sep 23, 2026 | Medline Industries recall: Convenience kits ANESTHESIA PAIN PK LEAGUE DYNJ67925A and 3 more productsMedical devices · 341; 459; 60; 336 | a sterility problem Serious | FDA Class II |
| Sep 23, 2026 | Medline Industries recall: Medline Convenience Kit: OPEN HEART A PACKMedical devices · 135 units | a sterility problem Serious | FDA Class II |
| Sep 9, 2026 | Medline Industries recall: Medline Convenience Kits containing BD ChloraPrep ClearMedical devices · 222,653 total | Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that wer… Serious | FDA Class II |
| Sep 9, 2026 | Medline Industries recall: Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT and 15 more productsMedical devices · 104 kits; 4636 kits; 58037 kits; 17,750 kits; 176 kits; 300 kits; 434,595 kits; 1840 kits; 22736 Kits; 3650 kits; 13032 kits; 3752 kits; 352 kits; 2080 kits; 18290 kits; 996692 kits | a sterility problem Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline medical convenience kit labeled as: TRACH TUBE KITMedical devices · 45 kits | Component labeling discrepancy Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline medical convenience kitsMedical devices · 2262 kits; 246 kits; 3468 kits; 974 kits | Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neuros… Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline Hudson RCI and 2 more productsMedical devices · 20 units; 145525 units; 271406 units | Neonatal and infant heated wire breathing circuits may experience sporadic failure. The he… Serious | FDA Class II |
| Sep 2, 2026 | Medline Industries recall: Medline convenience kits labeled as: 1) FEMORAL PACK and 10 more productsMedical devices · 71 kits; 263 kits; 24 kits; 94 kits; 15 kits; 663 kits; 1349 kits; 106 kits; 169 kits; 419 kits; 241 kits | Kits contain a potentially contaminated component which were recalled by the manufacturer Serious | FDA Class II |
| Aug 19, 2026 | Medline Industries recall: Medline Micro-Kill Bleach Germicidal Bleach WipesMedical devices · 591,561 units; 447,618 units; 1,244 units; 31,728 | Medline Micro-Kill Bleach Germicidal Bleach Wipes may exhibit a reduction in bleach concen… Serious | FDA Class II |
All 13 Medline Industries recalls →
FAQ
About this recall
Is Medline Industries Medline Convenience Kits: 1) KIT ANESTHESIA L&D A- LINE SET recalled?
Yes. Medline Industries, LP recalled it on August 11, 2026; FDA published it September 23, 2026 (Class I). Only the lots, dates or models listed on this page are included.
Why was it recalled?
The kits contain certain lots of sterile applicators which may contain fungal contamination that may occur under certain environmental conditions, allowing the growth of Aspergillus penicillioides. Contamination of skin preparation products with Aspergillus penicillioides may lead to serious adverse health consequences, including systemic infection, sepsis, illness, and death.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
Recalls
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.