Recall Register

Device recall: LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500

Class II FDA enforcement event 94356. Recall start date: . Status in the FDA record: Ongoing.

Reason for recall, in the words of FDA

A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.

Class II, in the words of FDA

a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote

MEDLINE INDUSTRIES, LP - Northfield started this device recall on 22 Mar 2024. The firm address in the FDA record is in Northfield, IL. FDA put the recall in Class II. FDA event 94356 has 21 product records. The first FDA enforcement report date is 28 Aug 2024. The record gives the status Ongoing.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.

Recalling firm

MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

21 product records in the event.

FDA event 94356: product records
Recall numberProductQuantityClassStatusReport date
Z-2694-2024LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500Class IIOngoing28 Aug 2024
Z-2695-2024LINER, SOFT, SUCTION CANISTER, 1500CC, REF OR929KClass IIOngoing28 Aug 2024
Z-2696-20241500ML SOFT LINER, 1/4X6 TBG NS, REF OR926KClass IIOngoing28 Aug 2024
Z-2697-20241,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR5392688703 unitsClass IIOngoing28 Aug 2024
Z-2698-20241,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR5392935900 unitsClass IIOngoing28 Aug 2024
Z-2699-20241,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG316125 unitsClass IIOngoing28 Aug 2024
Z-2700-2024Medline medical procedure kits labeled as follows: a) ANESTHESIA CIRCUIT ADULT, REF DYNJAAF6666B; b) ANESTHESIA CIRCUIT PEDS-LF, REF DYNJAP9918A; c) CV ANESTHESIA - ROOM SET UP, REF DYNJ905503F1920 unitsClass IIOngoing28 Aug 2024
Z-2701-2024Medline medical procedure kits labeled as follows: a) HEART ANESTHESIA SET UP, REF DYNJ902752C, b) KIT ENDO, REF DYKE1872A, c) LOWER ENDO KIT, REF DYKE1921A, d) PACEMAKER, REF DYNJ901681D, e) UPPER ENDO KIT, REF DYKE1922A, f) VASCULAR, REF DYNJ905515D, g) VASCUALR, REF DYNJ902387K, h) VASCULAR III, REF DYNJS2035C26096 unitsClass IIOngoing28 Aug 2024
Z-2702-2024Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A99 unitsClass IIOngoing28 Aug 2024
Z-2703-2024Medline medical procedure kits labeled as follows: a) BASIC NASAL, REF DYNJ909932; b) BRONCH KIT, REF DYKE1007B; c) ENT, REF DYNJ909935; d) NASAL SINUS-LF, REF DYNJ902624G; e) ORAL, REF DYNJ902377I; f) PACK,BRONCHOSCOPY, REF DYNJ65475B; g) PACK,HEAD AND NECK, REF DYNJ65487B; h) PACK,SINUS, REF DYNJ906898; i) PACK,T &…6998 unitsClass IIOngoing28 Aug 2024
Z-2704-2024Medline medical procedure kits labeled as follows: a) CYSTO, REF DYNJ905000D; b) ENDO KIT, REF DYKE1462A; c) ENDOSCOPY KIT, REF DYKE1431B; d) ENDOSCOPY KIT, REF DYKE1623B; e) GENERAL LAPAROSCOPY, REF DYNJ902385I; f) GENERAL LAPAROSCOPY, REF DYNJ905508G; g) GENERAL LAPAROSCOPY V, REF DYNJS2032D; h) LAP APPY, REF…22891 unitsClass IIOngoing28 Aug 2024
Z-2705-2024Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E12588 unitsClass IIOngoing28 Aug 2024
Z-2706-2024Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYKE1410A3400 unitsClass IIOngoing28 Aug 2024
Z-2707-2024Medline medical procedure kits labeled as follows: a) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, REF DYNJ905002B; c) SUCTION MEDI VAC, REF DYKM20333539 unitsClass IIOngoing28 Aug 2024
Z-2708-2024Medline medical procedure kits labeled as follows: a) AAA CDS, REF CDS984011C; b) CAN KIT, REF DYKM1184; c) DENTAL CDS, REF CDS984010B; d) EGD KIT, REF DYK1253578F; e) EGD REG KIT, REF DYKE1830; f) ENDO KIT, REF DYKE1516A; g) ERCP REG KIT, REF DYKM2127; h) GI PACK, REF DYKE1898; i) KIT, PEG, REG, REF DYKM2128; j)…75098 unitsClass IIOngoing28 Aug 2024
Z-2709-2024Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM21691700 unitsClass IIOngoing28 Aug 2024
Z-2710-2024Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F160 unitsClass IIOngoing28 Aug 2024
Z-2711-2024Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ9085662013 unitsClass IIOngoing28 Aug 2024
Z-2712-2024Medline medical procedure kits labeled as follows: a) GYN CDS, REF DYNJ905499B; b) GYN LAP, REF DYNJ909936; c) GYN LAPAROSCOPY, REF DYNJ902371J; d) GYN LAPAROSCOPY, REF DYNJ905509F; e) GYN LAPAROSCOPY II, REF DYNJS2030F; f) LAP ROBOTIC, REF DYNJ902384K; g) LAPAROSCOPY-ROBOT, REF DYNJ905003C; h) ROBOTIC, REF DYNJ907156A964 unitsClass IIOngoing28 Aug 2024
Z-2713-2024Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C1753 unitsClass IIOngoing28 Aug 2024
Z-2714-2024Medline medical procedure kits labeled as follows: a) ARTHROSCOPY, REF DYNJ909699; b) BACK CDS, REF CDS984000C; c) EXTREMITY, REF DYNJ900847A; d) HAND-LF, REF DYNJ902619G; e) HIP PINNING CDS, REF CDS984009C; f) HIP PINNING/TFN/ANTERIOR HIP, REF DYNJ902380K; g) KNEE, REF DYNJ904771B; h) KNEE ARTHROSCOPY, REF…14977 unitsClass IIOngoing28 Aug 2024

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class II: The middle of the three FDA recall classes.

The event in context

Device events that started in 2024
970
Share of these events in Class II
87%
Product records in this event
21Median of the firm: 2
Events of the firm on the register
120

Other events of the firm

Other FDA enforcement events of MEDLINE INDUSTRIES, LP - Northfield
InitiatedProduct (first record)TypeClassRecords
25 Jul 2025Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRDeviceClass I2
23 Jul 2025Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR DeviceClass II1
14 Jul 2025Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH,DeviceClass I1
8 Jul 2025The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utiliDeviceClass II1
7 Jul 2025Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, ManufDrugClass II6
16 Jun 2025SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301DeviceClass II1
12 Jun 2025Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564DeviceClass II4
23 May 2025Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER DeviceClass II3
15 May 2025Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250DeviceClass II1
22 Apr 2025Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS98DeviceClass I3

MEDLINE INDUSTRIES, LP - Northfield: all 120 events

Official channels

Cite this page

Recall Register. FDA enforcement event 94356. https://recallregister.com/fda/ii/94356/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA device enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: Worldwide - US Nationwide and the countries of Panama, Mexico, Canada, Qatar, El Salvador, Oman, Colombia, Singapore.
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many device recalls of 2024 have the same class?
87% of the 970 device events that started in 2024 are in Class II.
How many FDA recalls does MEDLINE INDUSTRIES, LP - Northfield have?
MEDLINE INDUSTRIES, LP - Northfield is the recalling firm in 120 enforcement events on this register. This event is 1 of them.