CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F recallZ-1824-2026 · Medline Industries, LP · initiated Mar 16, 2026
Class II Open, Classified All recalls posted in April 2026
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medline Industries, LP or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
FDA root cause category: Under Investigation by firm
What the company is doing
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].
Recall details
- Recall number
- Z-1824-2026
- Recall class
- Class II
- Status
- Open, Classified
- Initiated by the company
- Mar 16, 2026
- Posted by the FDA
- Apr 16, 2026
- Recalling firm
- Medline Industries, LP
- Quantity
- 640 kits
- Product code
- LRO
- FDA submissions
- K213481
- Distribution
- US Nationwide distribution in the state of South Carolina.
Product description
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
Code information (models, lots, serial numbers)
Medline Kit Number/SKU CIT7050F, UDI/DI each 10198459536656, UDI/DI case 40198459536657, Lot Number 25KLA002
Other devices under the same FDA submission
321 devices cleared under K213481 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.
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- MEDLINE ECVC6355Medline Industries, Inc. · General surgery tray3 recalls0 reports
- MEDLINE ECVC1045Medline Industries, Inc. · General surgery tray3 recalls0 reports
- Centurion ART255Centurion Medical Products Corporation · General surgery tray3 recalls0 reports
- Centurion CVI3880Centurion Medical Products Corporation · General surgery tray3 recalls0 reports
- MEDLINE ECVC1375Medline Industries, Inc. · General surgery tray3 recalls0 reports
- MEDLINE DYNDV2520Medline Industries, Inc. · General surgery tray3 recalls0 reports
- Centurion ST11670ACenturion Medical Products Corporation2 recalls0 reports
- Medline Industries, Inc. ECVC6370Centurion Medical Products Corporation · General Surgery Tray2 recalls0 reports
- MEDLINE ECVC6840Medline Industries, Inc. · General surgery tray2 recalls0 reports
- MEDLINE ECVC6265Medline Industries, Inc. · General Surgery Tray2 recalls0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 18, 2026. Text above is shown as published by the FDA.
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