Recall of CENTURION Circumcision Kit by Medline Industries
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Medline Industries is recalling 640 kits of the CENTURION Circumcision Kit due to improper sterilization, posing potential health risks.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on May 4, 2026 and geographically references United States, specifically South Carolina. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
Medline Industries, LP is recalling a lot of their CENTURION Circumcision Kit because it was distributed without the required sterilization process, making it not sterile.
Which Products Are Affected
The affected product is the CENTURION Circumcision Kit with Medline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, and Lot Number 25KLA002. A total of 640 kits are involved, distributed in the United States, specifically in South Carolina.
What You Should Do
Consumers who have the affected kits should contact Medline Industries, LP at their address: 3 Lakes Dr, Northfield, IL 60093-2753 for instructions on returns or refunds.
Why This Matters
This recall highlights potential health risks from non-sterile medical devices, which could lead to infections during procedures.
Source
FDA recall notice with recall number Z-1824-2026.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (895 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to May 4, 2026.
Frequently Asked Questions
Common questions about this FDA recall.