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Open, Classified

CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F

FDA Recall Z-1824-2026 · Posted 2026-04-16

Recalling FirmMedline Industries, LP
Recall StatusOpen, Classified
Product CodeLRO
Date Initiated2026-03-16
Product Quantity640 kits

Reason for Recall

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

Firm Action

Medline Industries, LP issued an URGENT MEDICAL DEVICE RECALL notice to its sole consignee on 3/16/2026 via email. The notice explained the issue, potential risk of use, and requested the destruction of the affected product. The firm was also directed to notify anyone to whom the product was further distributed. For questions, contact the Recall Department at 866-359-1704 or [email protected].

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide distribution in the state of South Carolina.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K213481Medline General Surgery TrayMedline Industries, Inc. · 2022-05-24

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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