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
31 of 31 products
| Model / number | Product as published |
|---|---|
CDS982407N | BAP NORTH ROBOTIC SURGERY CDS |
CDS985431K | TOT/ GYN LITHOTOMY CDS |
CDS985431O | TOT/ GYN LITHOTOMY CDS |
DYKMBNDL109A | KIT ROBOTICS GYN |
DYKMBNDL116A | KIT ROBOTICS UROLOGY PROSTATE |
DYKMBNDL116G | KIT ROBOTICS UROLOGY PROSTATE |
DYNJ04135B | ROBOTIC PACK |
DYNJ04382J | MINOR LITHOTOMY PACK |
DYNJ0665843C | NBMC D & C PACK-LF |
DYNJ22567G | D&C PACK-LF |
DYNJ22567J | D&C PACK-LF |
DYNJ41272B | D AND C |
DYNJ41272C | D AND C |
DYNJ42884 | OB PACK |
DYNJ47713A | D&C/GYN PACK |
DYNJ55377D | PERI GYN PACK |
DYNJ58344 | ANTERIOR CERVICAL-LF |
DYNJ67214D | D&C PACK |
DYNJ67214F | D&C PACK |
DYNJ67214G | D&C PACK |
- Lot codes and dates
131 of 131 products
Products covered by this recall # Barcodes Product as published 1 1019348968300440193489683005Lot Number: 21DBO201; 2) CDS982407N, UDI-DI: 10193489683004(each), 40193489683005(case) 2 1019532745129540195327451296Lot Number: 21CBD150; 3) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case) 3 1019532745129540195327451296Lot Number: 23GBM332; 4) CDS985431K, UDI-DI: 10195327451295(each), 40195327451296(case) 4 1019845919500640198459195007Lot Number: 23GBL932; 5) CDS985431O, UDI-DI: 10198459195006(each), 40198459195007(case) 5 1019348984877940193489848770Lot Number: 25GBB847; 6) DYKMBNDL109A, UDI-DI: 10193489848779(each), 40193489848770(case) 6 1019348984877940193489848770Lot Number: 21IBS290; 7) DYKMBNDL109A, UDI-DI: 10193489848779(each), 40193489848770(case) 7 1019348984877940193489848770Lot Number: 21GBE967; 8) DYKMBNDL109A, UDI-DI: 10193489848779(each), 40193489848770(case) 8 1019348984877940193489848770Lot Number: 21FBB105; 9) DYKMBNDL109A, UDI-DI: 10193489848779(each), 40193489848770(case) 9 1019348984877940193489848770Lot Number: 21DBC065; 10) DYKMBNDL109A, UDI-DI: 10193489848779(each), 40193489848770(case) 10 1019348988071740193489880718Lot Number: 21CBQ508; 11) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 11 1019348988071740193489880718Lot Number: 22HBE127; 12) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 12 1019348988071740193489880718Lot Number: 22GBL821; 13) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 13 1019348988071740193489880718Lot Number: 22FBM235; 14) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 14 1019348988071740193489880718Lot Number: 22FBC878; 15) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 15 1019348988071740193489880718Lot Number: 22EBP063; 16) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 16 1019348988071740193489880718Lot Number: 22EBP060; 17) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 17 1019348988071740193489880718Lot Number: 21KBQ697; 18) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 18 1019348988071740193489880718Lot Number: 21HBB549; 19) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 19 1019348988071740193489880718Lot Number: 21FBB101; 20) DYKMBNDL116A, UDI-DI: 10193489880717(each), 40193489880718(case) 20 1019845915699140198459156992Lot Number: 21DBE919; 21) DYKMBNDL116G, UDI-DI: 10198459156991(each), 40198459156992(case) - Amount recalled
- 7725 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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