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
36 of 36 products
| Model / number | Product as published |
|---|---|
CDS984086I | HYSTEROSCOPY |
DYKMBNDL91A | KIT GYN ONCOLOGY LAP |
DYNJ0373807J | VAGINAL HYSTERECTOMY PACK-LF |
DYNJ0373807K | VAGINAL HYSTERECTOMY PACK-LF |
DYNJ27434R | MINOR VAGINAL #76-RF |
DYNJ31344J | VAG HYST PACK |
DYNJ31344K | VAG HYST PACK |
DYNJ33393L | RRMC VAGINAL HYSTERECTOMY PACK |
DYNJ33393M | RRMC VAGINAL HYSTERECTOMY PACK |
DYNJ33393N | RRMC VAGINAL HYSTERECTOMY PACK |
DYNJ33393O | RRMC VAGINAL HYSTERECTOMY PACK |
DYNJ36712F | LAVH PACK |
DYNJ45090I | D&C MINOR LITHOTOMY PACK |
DYNJ45801C | D C HYSTEROSCOPY PACK-LF |
DYNJ47694I | VAG HYST PACK (VHGSG)642-LF |
DYNJ51741B | HYSTEROSCOPY D AND C PACK |
DYNJ58121C | LAVH - N #668629 -N |
DYNJ59037B | PK, GYN-MINOR-LITHO |
DYNJ59444G | HYSTEROSCOPY PACK |
DYNJ61282B | D AND C PACK |
- Lot codes and dates
105 of 105 products
Products covered by this recall # Barcodes Product as published 1 1019532742800640195327428007Lot Number: 24CBQ563; 2) CDS984086I, UDI-DI: 10195327428006(each), 40195327428007(case) 2 1019532742800640195327428007Lot Number: 24ABO363; 3) CDS984086I, UDI-DI: 10195327428006(each), 40195327428007(case) 3 1019532742800640195327428007Lot Number: 23IBV204; 4) CDS984086I, UDI-DI: 10195327428006(each), 40195327428007(case) 4 1019532742800640195327428007Lot Number: 23HBY878; 5) CDS984086I, UDI-DI: 10195327428006(each), 40195327428007(case) 5 1019532724689140195327246892Lot Number: 23GBE705; 6) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 6 1019532724689140195327246892Lot Number: 23HBI773; 7) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 7 1019532724689140195327246892Lot Number: 23FBD256; 8) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 8 1019532724689140195327246892Lot Number: 23FBC116; 9) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 9 1019532724689140195327246892Lot Number: 23CBS135; 10) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 10 1019532724689140195327246892Lot Number: 23CBL440; 11) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 11 1019532724689140195327246892Lot Number: 22KBH451; 12) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 12 1019532724689140195327246892Lot Number: 22KBH032; 13) DYKMBNDL91A, UDI-DI: 10195327246891(each), 40195327246892(case) 13 1019348994299640193489942997Lot Number: 22KBH028; 14) DYNJ0373807J, UDI-DI: 10193489942996(each), 40193489942997(case) 14 1019532722568140195327225682Lot Number: 22EBC904; 15) DYNJ0373807K, UDI-DI: 10195327225681(each), 40195327225682(case) 15 1019532722568140195327225682Lot Number: 22JBO175; 16) DYNJ0373807K, UDI-DI: 10195327225681(each), 40195327225682(case) 16 1019532710772740195327107728Lot Number: 22HBV873; 17) DYNJ27434R, UDI-DI: 10195327107727(each), 40195327107728(case) 17 1019348949660440193489496605Lot Number: 23EBQ683; 18) DYNJ31344J, UDI-DI: 10193489496604(each), 40193489496605(case) 18 1019348949660440193489496605Lot Number: 21LBL067; 19) DYNJ31344J, UDI-DI: 10193489496604(each), 40193489496605(case) 19 1019348949660440193489496605Lot Number: 21CBJ513; 20) DYNJ31344J, UDI-DI: 10193489496604(each), 40193489496605(case) 20 1019532708928340195327089284Lot Number: 21ABP592; 21) DYNJ31344K, UDI-DI: 10195327089283(each), 40195327089284(case) - Amount recalled
- 4415 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.
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.