Reported Sep 18, 2024 · Ongoing
Medline convenience kits containing semi-rigid suction liners labeled as follows
MEDLINE INDUSTRIES, LP - Northfield
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 - Northfield · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
Medline convenience kits containing semi-rigid suction liners labeled as follows
6 of 6 products
| # | Product as published |
|---|---|
| 1 | OPEN HEART KIT,ALTA BATES HOSP, Pack Number DYK1002174I |
| 2 | ENDO KIT, Pack Number DYKE1558B |
| 3 | ENDO KIT, Pack Number DYKE1804A |
| 4 | VASCULAR-LF, Pack Number DYNJ900714C |
| 5 | MAJOR CARDIOVASC ADULT, Pack Number DYNJ905472B |
| 6 | AV FISTULA, Pack Number DYNJ908096A |
- Lot codes and dates
12 of 12 products
Products covered by this recall # Barcodes Product as published 1 4019532733240310195327332402UDI/DI case 40195327332403, UDI/DI each 10195327332402 2 Lot Numbers: 24CLA959 3 4019532725851210195327258511DYKE1558B: UDI/DI case 40195327258512, UDI/DI each 10195327258511 4 Lot Numbers: 24DMA783, 24BMG878, 23LMG790 5 4019532702303510195327023034DYKE1804A: UDI/DI case 40195327023035, UDI/DI each 10195327023034 6 Lot Numbers: 24BMI437, 24AME311, 23LMC958 7 4019348995136410193489951363DYNJ900714C: UDI/DI case 40193489951364, UDI/DI each 10193489951363 8 Lot Numbers: 24FBC609 9 4019532720057310195327200572DYNJ905472B: UDI/DI case 40195327200573, UDI/DI each 10195327200572 10 Lot Numbers: 24BBS291 11 4019532750706110195327507060DYNJ908096A: UDI/DI case 40195327507061, UDI/DI each 10195327507060 12 Lot Numbers: 24ABX948, 24ABB080 - Amount recalled
- 1,646 units
This recall covers 106 products
The agency filed one notice per product. You are reading one of them; the other 105 are below.
93 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.
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.
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