Z-2042-2026Class II

Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL...

Name: Z-2042-2026 Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL...
Creator: Medline Industries, LP
Published: 2026-03-16
License: https://open.fda.gov/license/

MEDLINE INDUSTRIES, LP - Northfield / initiated 2026-03-16 / Open, Classified / root cause: sterility

FDA source

Medline Industries, LP began a recall of Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL PURPOSE TRAY, Medline Kit SKU 75670 on 2026-03-16. FDA classified it as Class II and gives the reason as "Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as sterility.

Recall record

Recall number: Z-2042-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-03-16
Posted: 2026-04-30
Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Product: Centurion medical convenience kits, containing Webcol Large Alcohol Prep Pads, labeled as: LATEX FREE GENERAL PURPOSE TRAY, Medline Kit SKU 75670
Product code: LRP Tray, Surgical
Reason for recall: Medline Industries, LP is issuing a recall for specific item(s) and lot(s) of Medline Kits containing Cardinal Health Webcol Large Alcohol Prep Pads. Cardinal Health has deemed Webcol Large Alcohol Prep Pads to be non-sterile following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.
Root cause tag: sterility
FDA root cause: Under Investigation by firm
Action: Medline Industries, LP issued an URGENT MEDICAL DEVICE RECALL notice to its consignees on 3/16/2026 via USPS first class mail and email. The notice explained the issue, potential risk, and requested the affected product be quarantined pending additional labeling. Consignees were directed to respond to the notice via Website link: https://recalls.medline.com, and upon receipt of the submitted response form, the account will receive over-labels to place on affected inventory, with instructions for the user to remove and discard the affected component prior to using the kit. These labels will be provided via FedEx overnight. Distributors or those who have further distributed the product are directed to notify those receiving the affected kits, and to include the customers quantities on the response form. Upon receipt of your submitted response form, you will receive over-labels to provide to the customers to affix to their affected product. For questions, contact the Recall Department at 866-359-1704 or [email protected].
Quantity in commerce: 1590 kits
Distribution: US Nationwide distribution.
Product codes and lots: UDI/DI each 00653160095890, UDI/DI case 10653160095897, Lot Number: 2025102290

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2042-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2039-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2040-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2041-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2042-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2043-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2044-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30
Z-2045-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-05-06	2026-04-30

Product code LRP

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)