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
18 of 18 products
| # | Product as published |
|---|---|
| 1 | ENDO KIT, Pack Number DYKE1092B |
| 2 | VIDEO BRONCHOSCOPY TRAY, Pack Number DYKE1666 |
| 3 | SUCTION CANISTER KIT, Pack Number DYKM2196 |
| 4 | SUCTION CANISTER KIT, Pack Number DYKM2196H |
| 5 | BRONCH LAB PACK-LF, Pack Number DYNJ24810B |
| 6 | THORACIC, Pack Number DYNJ907991F |
| 7 | RECTAL, Pack Number DYNJ908108A |
| 8 | ROBOTIC, Pack Number DYNJ908109C |
| 9 | CERVICAL, Pack Number DYNJ908748D |
| 10 | LAMI, Pack Number DYNJ908750D |
| 11 | MERCY TIFFIN BASIC-LF, Pack Number DYNJ909731 |
| 12 | MERCY TIFFIN LITHOTOMY, Pack Number DYNJ909735 |
| 13 | BASIC GENERAL SET UP, Pack Number DYNJ909945 |
| 14 | BASIC GENERAL SET UP, Pack Number DYNJ909945A |
| 15 | AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289 |
| 16 | AMB OCULOPLASTICS MUSC, Pack Number DYNJ910289H |
| 17 | MTHZ TOTAL HIP, Pack Number DYNJC9311M |
| 18 | BRONCH KIT, Pack Number P906877 |
- Lot codes and dates
18 of 18 products
Products covered by this recall # Barcodes Product as published 1 40889942777366UDI/DI case 40889942777366, UDI/DI each10889942777365, Lot Numbers: 24BBK418, 24DBH210 2 40193489708487DYKE1666: UDI/DI case 40193489708487, UDI/DI each10193489708486, Lot Numbers: 24ADB503, 24CDA282, 24CDB279, 24DDB221, 24EDA406 3 40195327236916DYKM2196: UDI/DI case 40195327236916, UDI/DI each10195327236915, Lot Numbers: 23LBF762, 24BBB541, 24CBI973, 24DBH448 4 40195327236916DYKM2196H: UDI/DI case 40195327236916, UDI/DI each10195327236915, Lot Numbers: 23LBF762, 24BBB541, 24CBI973, 24DBH448 5 40889942440611DYNJ24810B: UDI/DI case 40889942440611, UDI/DI each10889942440610, Lot Numbers: 24CBE214 6 40195327641468DYNJ907991F: UDI/DI case 40195327641468, UDI/DI each10195327641467, Lot Numbers: 24DLA042, 24DLA594 7 40195327507153DYNJ908108A: UDI/DI case 40195327507153, UDI/DI each10195327507152, Lot Numbers: 24BBK532 8 40195327507238DYNJ908109C: UDI/DI case 40195327507238, UDI/DI each10195327507237, Lot Numbers: 23LBT867, 24BBA187, 24DBI723, 24FBA058 9 40195327549207DYNJ908748D: UDI/DI case 40195327549207, UDI/DI each10195327549206, Lot Numbers: 23LBE394, 24CBD863 10 40195327549214DYNJ908750D: UDI/DI case 40195327549214, UDI/DI each10195327549213, Lot Numbers: 24FBC284 11 40195327464524DYNJ909731: UDI/DI case 40195327464524, UDI/DI each10195327464523, Lot Numbers: 24ABU492 12 40195327464685DYNJ909735: UDI/DI case 40195327464685, UDI/DI each10195327464684, Lot Numbers: 23LBH989, 24ABV099, 24CBG700 13 40195327512669DYNJ909945: UDI/DI case 40195327512669, UDI/DI each10195327512668, Lot Numbers: 24ABV895 14 40195327615803DYNJ909945A: UDI/DI case 40195327615803, UDI/DI each10195327615802, Lot Numbers: 24DBA530 15 40195327618675DYNJ910289: UDI/DI case 40195327618675, UDI/DI each10195327618674, Lot Numbers: 24CBC847 16 40198459012489DYNJ910289H: UDI/DI case 40198459012489, UDI/DI each10198459012488, Lot Numbers: 24CBC847 17 40198459012489DYNJC9311M: UDI/DI case 40198459012489, UDI/DI each10198459012488, Lot Numbers: 24FDA111 18 40889942002581P906877: UDI/DI case 40889942002581, UDI/DI each10889942002580, Lot Numbers: 24FDA021 - Amount recalled
- 3117 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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