Recall archive / FDA device enforcement
Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMI... — FDA record Z-1191-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 12, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Medline medical procedure convenience kits labeled as: 1) SMJ LAP CHOLE PACK-LF, Kit SKU DYNJ19974P; 2) DEPAUL ABDOMINAL ENDOSCOPY-LF, Kit SKU DYNJ20027K; 3) LAPAROSCOPY PACK-LF, Kit SKU DYNJ20468J; 4) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763N; 5) SMJ LAPAROSCOPY PACK, Kit SKU DYNJ25763O; 6) BWNBORO LAP CHOLE PACK-LF, Kit SKU DYNJ32836B; 7) MINOR SET UP PACK, Kit SKU DYNJ43272K; 8) PK, GEN LAPAROSCOPIC CHOLE, Kit SKU DYNJ43976C; 9) GV LAP CHOLE PACK, Kit SKU DYNJ46939Q; 10) LAP CHOLE PACK, Kit SKU DYNJ49688C; 11) GENERAL ROBOTIC LAP, Kit SKU DYNJ51347N; 12) LAP CHOLE PACK, Kit SKU DYNJ54081F; 13) PEDIATRIC MOSES, Kit SKU DYNJ58864B; 14) LAPAROTOMY PACK, Kit SKU DYNJ59313B; 15) CRMC LAP CHOLE DIAG LAP-LF, Kit SKU DYNJ61095F; 16) LAP GASTRIC PACK, Kit SKU DYNJ62065A; 17) MINOR PACK, Kit SKU DYNJ64174A; 18) GENERAL SURGERY PACK, Kit SKU DYNJ64258I; 19) GENERAL LAP SHARED-LF, Kit SKU DYNJ64786D; 20) CHOLE PACK, Kit SKU DYNJ67686B; 21) GEN SURG MINOR PACK, Kit SKU DYNJ69142F; 22) LAP CHOLE PACK, Kit SKU DYNJ81695B; 23) GENERAL LAPAROSCOPY, Kit SKU DYNJ900901K; 24) GEN MINOR, Kit SKU DYNJ900906L; 25) ROBOTIC GENERAL, Kit SKU DYNJ906861D; 26) RMC GENERAL LAPAROSCOPIC, Kit SKU DYNJ907087C; 27) LAP CHOLE LMC CDS, Kit SKU DYNJ911116A; 28) MINOR GENERAL PACK, Kit SKU DYNJT3884; 29) GENERAL LAPAROSCOPY PACK, Kit SKU DYNJT4504; 30) MINOR SURGERY PACK-LF, Kit SKU PHS109062D.
- Reason
- Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
- Classification
- Class II
- Recalling firm
- Medline Industries, LP
- Quantity
- 456 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1191-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Medline Kit SKU DYNJ19974P: UDI/DI 10198459138195 (EA) 40198459138196 (CS), Lot Number 25KMB830; Medline Kit SKU DYNJ19974P: UDI/DI 10198459138195 (EA) 40198459138196 (CS), Lot Number 25KMB831; Medline Kit SKU DYNJ20027K: UDI/DI 10198459228957 (EA) 40198459228958 (CS), Lot Number 25KMG395; Medline Kit SKU DYNJ20027K: UDI/DI 10198459228957 (EA) 40198459228958 (CS), Lot Number 25KMH132; Medline Kit SKU DYNJ20468J: UDI/DI 10195327024338 (EA) 40195327024339 (CS), Lot Number 25KMF540; Medline Kit SKU DYNJ25763N: UDI/DI 10198459138218 (EA) 40198459138219 (CS), Lot Number 25KMH134; Medline Kit SKU DYNJ25763O: UDI/DI 10198459603655 (EA) 40198459603656 (CS), Lot Number 25KMI209; Medline Kit SKU DYNJ32836B: UDI/DI 10195327037369 (EA) 40195327037360 (CS), Lot Number 25KBF167; Medline Kit SKU DYNJ43272K: UDI/DI 10198459257131 (EA) 40198459257132 (CS), Lot Number 25KME892; Medline Kit SKU DYNJ43976C: UDI/DI 10193489806694 (EA) 40193489806695 (CS), Lot Number 25KMG962; Medline Kit SKU DYNJ46939Q: UDI/DI 10198459404047 (EA) 40198459404048 (CS), Lot Number 25JDA437; Medline Kit SKU DYNJ46939Q: UDI/DI 10198459404047 (EA) 40198459404048 (CS), Lot Number 25LDA059; Medline Kit SKU DYNJ49688C: UDI/DI 10198459155017 (EA) 40198459155018 (CS), Lot Number 25KMG180; Medline Kit SKU DYNJ51347N: UDI/DI 10198459386428 (EA) 40198459386429 (CS), Lot Number 25JBW506; Medline Kit SKU DYNJ54081F: UDI/DI 10198459172410 (EA) 40198459172411 (CS), Lot Number 25KMB295; Medline Kit SKU DYNJ58864B: UDI/DI 10198459346965 (EA) 40198459346966 (CS), Lot Number 25JBW678; Medline Kit SKU DYNJ59313B: UDI/DI 10195327248338 (EA) 40195327248339 (CS), Lot Number 25JMJ736; Medline Kit SKU DYNJ61095F: UDI/DI 10198459228568 (EA) 40198459228569 (CS), Lot Number 25KMC402; Medline Kit SKU DYNJ62065A: UDI/DI 10193489273472 (EA) 40193489273473 (CS), Lot Number 25KMI773; Medline Kit SKU DYNJ64174A: UDI/DI 10198459076367 (EA) 40198459076368 (CS), Lot Number 25LMB281; Medline Kit SKU DYNJ64258I: UDI/DI 10198459031564 (EA) 40198459031565 (CS), Lot Number 25KMJ665; Medline Kit SKU DYNJ64786D: UDI/DI 10198459328671 (EA) 40198459328672 (CS), Lot Number 25JMJ978; Medline Kit SKU DYNJ67686B: UDI/DI 10198459383120 (EA) 40198459383121 (CS), Lot Number 25KMH683; Medline Kit SKU DYNJ69142F: UDI/DI 10198459478499 (EA) 40198459478490 (CS), Lot Number 25KMH891; Medline Kit SKU DYNJ81695B: UDI/DI 10198459023453 (EA) 40198459023454 (CS), Lot Number 25KMB850; Medline Kit SKU DYNJ900901K: UDI/DI 10198459272493 (EA) 40198459272494 (CS), Lot Number 25KBP907; Medline Kit SKU DYNJ900906L: UDI/DI 10198459408526 (EA) 40198459408527 (CS), Lot Number 25LMA386; Medline Kit SKU DYNJ906861D: UDI/DI 10198459293702 (EA) 40198459293703 (CS), Lot Number 25LMA703; Medline Kit SKU DYNJ907087C: UDI/DI 10198459201301 (EA) 40198459201302 (CS), Lot Number 25KMJ480; Medline Kit SKU DYNJ911116A: UDI/DI 10198459354274 (EA) 40198459354275 (CS), Lot Number 25KMH214; Medline Kit SKU DYNJ911116A: UDI/DI 10198459354274 (EA) 40198459354275 (CS), Lot Number 25KMJ766; Medline Kit SKU DYNJT3884: UDI/DI 10198459366840 (EA) 40198459366841 (CS), Lot Number 25JBX326; Medline Kit SKU DYNJT4504: UDI/DI 10198459456701 (EA) 40198459456702 (CS), Lot Number 25KMF188; Medline Kit SKU PHS109062D: UDI/DI 10889942716548 (EA) 40889942716549 (CS), Lot Number 25KMD005. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US Nationwide distribution.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Feb 4, 2026
- Recall initiation date
- Dec 12, 2025
- Center classification date
- Jan 28, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.