CLASS II ONGOING Device recall · Reported 22 Apr 2026 · FDA Enforcement Report

Centurion Circumcision Kit, Medline Kit Number recalled

Medline Industries is recalling Centurion Circumcision Kit, Medline Kit Number, distributed nationwide in the US. The recall was initiated on 16 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMedline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, Lot Number 25KLA002

Quantity recalled640 kits

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1824-2026
FDA event ID: 98626
Recalling firm: Medline Industries, Northfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 16 Mar 2026
FDA classified: 16 Apr 2026
Reported: 22 Apr 2026
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Sterility
Device type: Other Medical Devices

Timeline

16 Mar 2026	Recall initiated by company
16 Apr 2026	Classified by FDA	+31 days
22 Apr 2026	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F

Where it was distributed

US Nationwide distribution in the state of South Carolina.

Nationwide South Carolina

Questions about this recall

Is Centurion Circumcision Kit, Medline Kit Number recalled?

Yes. Medline Industries recalled Centurion Circumcision Kit, Medline Kit Number on 16 Mar 2026. The recall is Class II and its status is Ongoing. Recall number Z-1824-2026.

Why was it recalled?

On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.

Which lots are affected?

Medline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, Lot Number 25KLA002

Where was it sold?

US Nationwide distribution in the state of South Carolina.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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