Food, drugs, devices › MEDLINE INDUSTRIES, LP - Northfield

Device recall: MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES, Model numbers MSC351420AN, MSC351420ANH, MSC351420ANZ, MSC351430A, MSC351430

FDA enforcement event 90558 · Class II · initiated 29 Jun 2022 · status Ongoing

DeviceVoluntary: Firm initiated1 product recordNorthfield, IL

MEDLINE INDUSTRIES, LP - Northfield (Northfield, IL) initiated this device recall on 29 Jun 2022; FDA lists 1 product record under event 90558, classified Class II.

FDA defines Class II as 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. 88% of the 839 device enforcement events initiated in 2022 carry the same class.

Status: Ongoing. Initiation: voluntary: firm initiated. MEDLINE INDUSTRIES, LP - Northfield has 120 enforcement events on this register, with a median of 2 product records per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL.

Reason for recall

"stability failure"

Distribution

"US Nationwide distribution."

Product records

Recall number	Product	Quantity	Class	Status	Report date
Z-1493-2022	MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES, Model numbers MSC351420AN, MSC351420ANH, MSC351420ANZ, MSC351430A, MSC351430AZ	6119500 wipes	Class II	Ongoing	10 Aug 2022

Context

88%of 2022 device events are Class II839 events that year

1product record in this eventfirm median: 2

120events on this register for the firm

Other enforcement events for MEDLINE INDUSTRIES, LP - Northfield

Initiated	Product (first record)	Type	Class	Records
25 Jul 2025	Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TR	Device	Class I	2
23 Jul 2025	Medline Kits containing BD SureStep Foley Tray Systems: SKU/Description: CDS984076J GYN ROBOTIC DYNJG001004A LAVH MINOR	Device	Class II	1
14 Jul 2025	Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH,	Device	Class I	1
8 Jul 2025	The Medline General Surgery Tray is customized to meet requirements of the hospitals and health care professionals utili	Device	Class II	1
7 Jul 2025	Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manuf	Drug	Class II	6
16 Jun 2025	SwabFlush Prefilled Syringe with ICU Medical SwabCaps, 10mL Model no. EMZE010301	Device	Class II	1
12 Jun 2025	Medline Convenience Kits, containing BD ChloraPrep Clear - 1mL Applicator, labeled as: LABOR TRIAGE KIT, REF DYKM1564	Device	Class II	4
23 May 2025	Medline convenience kits containing BD Insyte Autoguard Shielded IV Catheters 22 GA x 1.00 IN. labeled as: 1) CC DRAWER	Device	Class II	3
15 May 2025	Medline UMBILICAL TRAY W/3.5&5FR CATH, REF UVT1250	Device	Class II	1
22 Apr 2025	Medline Kits containing Codman Disposable Perforator 14 mm: 1. CRANI ADD A PACK, SKU DYNJ30926O 2. CRANIOTOMY, SKU CDS98	Device	Class I	3

All 120 events for MEDLINE INDUSTRIES, LP - Northfield

Questions and answers

Why was this device recalled?

FDA's record gives the reason for recall as: "stability failure"

What does Class II mean?

FDA classifies recalls by relative degree of health hazard. Class II is 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.

Where was the product distributed?

FDA's distribution pattern field reads: "US Nationwide distribution."

Is the recall still ongoing?

FDA lists the status as Ongoing. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.