Recall Z-1824-2026— Medline Industries, LP
Class II · Ongoing
Class II FDA medical device recall by Medline Industries, LP, initiated 2026-03-16. It names one FDA 510(k) clearance: K213481. Product: CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F. Reason: On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile..
- Recalling firm
- Medline Industries, LP
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-03-16
- Firm location
- Northfield, IL, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Reason for recall
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
Data sourced from openFDA. This site is unofficial and independent of the FDA.