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.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-2694-2024 | LINER, SOFT, SUCTION CANISTER, 1500CC, REF DYNDSCL1500 | Class II | Ongoing | 28 Aug 2024 | |
| Z-2695-2024 | LINER, SOFT, SUCTION CANISTER, 1500CC, REF OR929K | Class II | Ongoing | 28 Aug 2024 | |
| Z-2696-2024 | 1500ML SOFT LINER, 1/4X6 TBG NS, REF OR926K | Class II | Ongoing | 28 Aug 2024 | |
| Z-2697-2024 | 1,5L MED-SOFT LINER W/ 6MMX1,8M TUB. & ADULT VC, REF OR53926 | 88703 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2698-2024 | 1,5L MED-SOFT LINER W/ 6MMX3M TUB. & ADULT VC, REF OR53929 | 35900 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2699-2024 | 1,5L MED-SOFT SINGLE LINER WITH SOLIDIFIER, REF OR1920PG | 316125 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2700-2024 | Medline 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 DYNJ905503F | 1920 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2701-2024 | Medline 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 DYNJS2035C | 26096 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2702-2024 | Medline medical procedure kits labeled as follows: DENTAL, REF DYNJ909211A | 99 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2703-2024 | Medline 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 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2704-2024 | Medline 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 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2705-2024 | Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYK1012268E1 | 2588 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2706-2024 | Medline medical procedure kits labeled as follows: a) ENDO KIT, REF DYKE1410A | 3400 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2707-2024 | Medline medical procedure kits labeled as follows: a) MAJOR BREAST, REF DYNJ905004C; b) MINOR BREAST, REF DYNJ905002B; c) SUCTION MEDI VAC, REF DYKM2033 | 3539 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2708-2024 | Medline 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 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2709-2024 | Medline medical procedure kits labeled as follows: a) KIT CANISTER SUCT W 12FT, REF DYKM2169 | 1700 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2710-2024 | Medline medical procedure kits labeled as follows: a) TURNOVER KIT, REF DYKC1289F | 160 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2711-2024 | Medline medical procedure kits labeled as follows: a) BASIC NEURO, REF DYNJ909171A; b) NEURO, REF DYNJ905510D; c) NEURO, REF DYNJ902388L; d) NEURO SAS, REF DYNJ908566 | 2013 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2712-2024 | Medline 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 DYNJ907156A | 964 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2713-2024 | Medline medical procedure kits labeled as follows: a) C-SECTION CDS, REF CDS983998C | 1753 units | Class II | Ongoing | 28 Aug 2024 |
| Z-2714-2024 | Medline 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 units | Class II | Ongoing | 28 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
Official channels
- FDA enforcement report Z-2694-2024The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA MedWatchThe FDA safety reporting program for drugs and medical devices.
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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.