Reported Feb 25, 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
16 of 16 products
| Model / number | Product as published |
|---|---|
DYKM1801B | TOTE ABRAMS KNEE ARTHROSCOPY |
DYKM1776 | TOTE SEN OSC HAND REPAIR |
DYKM1765A | TOTE MOMENI SB CAPSULOTOMY REC |
DYKM1796A | TOTE YAO OSC HAND REPAIR |
DYKM1756A | TOTE SB NGUYEN CAPSULOTOMY |
DYKM1783A | TOTE FOX OSC HAND REPAIR |
DYKM1730A | TOTE KAMAL OSC HAND REPAIR |
DYKM1927A | TOTE SB NGUYEN LIPOSUCTION |
DYKM1807 | TOTE YAO OSC WRIST ARTHROSCOPY |
DYKM1781A | TOTE CURTIN OSC HAND REPAIR |
DYKM1977B | OSC SHERMAN KNEE ARTHRO BASIC |
DYKM1751A | TOTE CHANGE OSC HAND REPAIR |
DYKM1864 | TOTE CARROLL BLOCK BLOOD PATCH |
DYKM1925 | TOTE SB STONE JWIRE LUMPECTOMY/SEN NODE |
DYKM1767B | TOTE SAFRAN OSC HIP ARTHRSCPY |
CVI4500A | CVC PACK |
- Lot codes and dates
47 of 47 products
Products covered by this recall # Barcodes Product as published 1 1088827773379420888277733791Lot Number: 2024100790; 2) DYKM1776, UDI-DI: 10888277733794(each), 20888277733791(case) 2 1019348919023620193489190233Lot Number: 2025013190; 3) DYKM1765A, UDI-DI: 10193489190236(each), 20193489190233(case) 3 1065316035488800653160354881Lot Number: 2024071790; 4) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) 4 1019348919025020193489190257Lot Number: 2024072390; 5) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 5 1019348919025020193489190257Lot Number: 2024080190; 6) DYKM1756A, UDI-DI: 10193489190250(each), 20193489190257(case) 6 1065316035488800653160354881Lot Number: 2024101490; 7) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) 7 1019348911133020193489111337Lot Number: 2025010890; 8) DYKM1783A, UDI-DI: 10193489111330(each), 20193489111337(case) 8 1019348911101920193489111016Lot Number: 2025011090; 9) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 9 1065316035488800653160354881Lot Number: 2025012890; 10) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) 10 1019348919990120193489199908Lot Number: 2025020690; 11) DYKM1927A, UDI-DI: 10193489199901(each), 20193489199908(case) 11 1019348911101920193489111016Lot Number: 2024012590; 12) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 12 1065316035488800653160354881Lot Number: 2024030690; 13) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) 13 1019348911101920193489111016Lot Number: 2024041790; 14) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 14 1019348911133020193489111337Lot Number: 2024052290; 15) DYKM1783A, UDI-DI: 10193489111330(each), 20193489111337(case) 15 1019348911101920193489111016Lot Number: 2024053190; 16) DYKM1730A, UDI-DI: 10193489111019(each), 20193489111016(case) 16 1065316035488800653160354881Lot Number: 2024060590; 17) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) 17 1019348911133020193489111337Lot Number: 2024061890; 18) DYKM1783A, UDI-DI: 10193489111330(each), 20193489111337(case) 18 1019348919121920193489191216Lot Number: 2024062890; 19) DYKM1807, UDI-DI: 10193489191219(each), 20193489191216(case) 19 1065316035273000653160352733Lot Number: 2024071990; 20) DYKM1781A, UDI-DI: 10653160352730(each), 00653160352733(case) 20 1065316035488800653160354881Lot Number: 2024092390; 21) DYKM1796A, UDI-DI: 10653160354888(each), 00653160354881(case) - Amount recalled
- 1496 units
This recall covers 43 products
The agency filed one notice per product. You are reading one of them; the other 42 are below.
30 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.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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