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

5 of 5 products

Products covered by this recall
#Product as published
1ANESTHESIA CIRCUIT-LF, Pack Number DYNJAA0311C
2ANESTHESIA CIRCUIT-LF, Pack Number DYNJAA0323C
3ANESTHESIA CIRCUIT ADULT, Pack Number DYNJAA0378A
4ADULT ANESTHESIA CIRC LAGUNA, Pack Number DYNJAA10579
5BREATHING CIRCUIT # 34827, Pack Number DYNJAAF6674I
Lot codes and dates

5 of 5 products

Products covered by this recall
#BarcodesProduct as published
14019348934351010193489343519UDI/DI case: 40193489343510, UDI/DI each 10193489343519, Lot Numbers: 24DBV950, 24CBL800, 24BBI902, 23LBT319
24019532742369910195327423698DYNJAA0323C: UDI/DI case 40195327423699, UDI/DI each 10195327423698, Lot Numbers: 24DBM735, 24DBN216, 24CBI422, 24CBJ132, 23KBU156
34019532745004610195327450045DYNJAA0378A: UDI/DI case 40195327450046, UDI/DI each 10195327450045, Lot Numbers: 24DBQ840, 24DBQ839, 24DBB513, 24ABM732, 24ABU331, 24ABU330, 24ABQ036, 24ABK802, 24ABF565, 24ABG771, 23LBN692, 23LBL609, 23KBU727
410889942600748DYNJAA10579: UDI/DI casev40889942600749, UDI/DI unit 10889942600748, Lot Numbers: 23LBL288
54019532738162310195327381622DYNJAAF6674I: UDI/DI case 40195327381623, UDI/DI each 10195327381622, Lot Numbers: 24DBM458, 24CBS798, 24CBO294, 23LBV673
Amount recalled
29,585 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.