Reported May 13, 2026 · Ongoing
Medline Convenience Kits
Medline Industries, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline Convenience Kits
17 of 17 products
| Model / number | Product as published |
|---|---|
CVI4500A | CVC PACK |
DYKM1730A | TOTE KAMAL OSC HAND REPAIR |
DYKM1751A | TOTE CHANGE OSC HAND REPAIR |
DYKM1756A | TOTE SB NGUYEN CAPSULOTOMY |
DYKM1765A | TOTE MOMENI SB CAPSULOTOMY REC |
DYKM1767B | TOTE SAFRAN OSC HIP ARTHRSCPY |
DYKM1776 | TOTE SEN OSC HAND REPAIR |
DYKM1781A | TOTE CURTIN OSC HAND REPAIR |
DYKM1783A | TOTE FOX OSC HAND REPAIR |
DYKM1796A | TOTE YAO OSC HAND REPAIR |
DYKM1801B | TOTE ABRAMS KNEE ARTHROSCOPY |
DYKM1807 | TOTE YAO OSC WRIST ARTHROSCOPY |
DYKM1864 | TOTE CARROLL BLOCK BLOOD PATCH |
DYKM1925 | TOTE SB STONE JWIRE LUMPECTOMY/SEN NODE |
DYKM1927A | TOTE SB NGUYEN LIPOSUCTION |
DYKM1977B | OSC SHERMAN KNEE ARTHRO BASIC |
DYKM2131 | CHEST TUBE SUPPLIES |
- Lot codes and dates
48 of 48 products
Products covered by this recall # Barcodes Product as published 1 1019348911101920193489111016Lot Number: 2020121550; 2) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 2 1019348911101920193489111016Lot Number: 2024030690; 3) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 3 1019348911101920193489111016Lot Number: 2024052290; 4) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 4 1019348911101920193489111016Lot Number: 2024060590; 5) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 5 1019348911100220193489111009Lot Number: 2025012890; 6) DYKM1751A, UDI-DI: 10193489111002(each), 20193489111009(case) 6 1019348919025020193489190257Lot Number: 2023121190; 7) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 7 1019348919025020193489190257Lot Number: 2023060290; 8) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 8 1019348919025020193489190257Lot Number: 2023070590; 9) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 9 1019348919025020193489190257Lot Number: 2023111590; 10) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 10 1019348919025020193489190257Lot Number: 2023120590; 11) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 11 1019348919025020193489190257Lot Number: 2024022190; 12) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 12 1019348919025020193489190257Lot Number: 2024080190; 13) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 13 1019348919023620193489190233Lot Number: 2024101490; 14) DYKM1765A, UDI-DI: 10193489190236(each), 20193489190233(case) 14 1019348919023620193489190233Lot Number: 2023050490; 15) DYKM1765A, UDI-DI: 10193489190236(each), 20193489190233(case) 15 1019348919023620193489190233Lot Number: 2023071290; 16) DYKM1765A, UDI-DI: 10193489190236(each), 20193489190233(case) 16 1019348919023620193489190233Lot Number: 2024012490; 17) DYKM1765A, UDI-DI: 10193489190236(each), 20193489190233(case) 17 1019348911236820193489112365Lot Number: 2024071790; 18) DYKM1767B, UDI-DI: 10193489112368(each), 20193489112365(case) 18 1088827773379420888277733791Lot Number: 2023102790; 19) DYKM1776, UDI-DI: 10888277733794(each), 20888277733791(case) 19 1088827773379420888277733791Lot Number: 2024031590; 20) DYKM1776, UDI-DI: 10888277733794(each), 20888277733791(case) 20 10653160352730653160352733Lot Number: 2025013190; 21) DYKM1781A, UDI-DI: 10653160352730(each), 653160352733(case) - Amount recalled
- 1516 units
This recall covers 42 products
The agency filed one notice per product. You are reading one of them; the other 41 are below.
29 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Medline Industries, LP recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.