Reported Jun 24, 2026 · Ongoing
MEDLINE Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR…
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 Medical Procedure Kits labeled as CLOVIS HYSTEROSCOPY, CSC-N PELVISCOPY, D AND C PACK, D&C HYSTER PACK, FLWR GYN PACK, FS LAP TUBAL LIGATION, HILLSDALE D&C / HYSTEROSCOPY, LAVH NEW BRAUNFELS,TVH PACK, etc (see recall documents for a full list of affected products)
- Lot codes and dates
293 of 293 products
Products covered by this recall Model / number Barcodes Product as published DYNJ61063A1019348964045840193489640459Medline Kit Number/ : UDI/DI 10193489640458 (each), 40193489640459 (case), Lot Number 21KBV571 DYNJ61063B1019532719347840195327193479Medline Kit Number/ : UDI/DI 10195327193478 (each), 40195327193479 (case), Lot Number 23EBU351 DYNJ61063B1019532719347840195327193479Medline Kit Number/ : UDI/DI 10195327193478 (each), 40195327193479 (case), Lot Number 23DBQ190 DYNJ61063B1019532719347840195327193479Medline Kit Number/ : UDI/DI 10195327193478 (each), 40195327193479 (case), Lot Number 23BBE364 DYNJ61063B1019532719347840195327193479Medline Kit Number/ : UDI/DI 10195327193478 (each), 40195327193479 (case), Lot Number 22IBW094 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 26CMK666 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 26BMG709 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 26AMI644 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25KMD133 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25JMA568 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25IMF717 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25HMJ595 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25FMH149 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25EME964 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25DMG466 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25CMH227 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25CMC736 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 25BMB744 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 24LMB964 DYNJ61063C1019532745168440195327451685Medline Kit Number/ : UDI/DI 10195327451684 (each), 40195327451685 (case), Lot Number 24JMB516 - Amount recalled
- 37324 units
This recall covers 64 products
The agency filed one notice per product. You are reading one of them; the other 63 are below.
51 more are in the archive.
Where it was sold
Why it was recalled
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
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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