Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
241-McKesson Premium Skin Staple Remover Kit Recalled by Cypress Medical Products LLC Due to Product not meeting the iodine assay level requirements...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cypress Medical Products LLC directly.
Affected Products
241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal Kit, and 82-15 Cypress Medical Products Skin Staple Remover Kit. McKesson Item # 241, 100123, and 100124, Cypress Item # 82-15 Manual surgical instrument for general use.
Quantity: 12,206 cases
Why Was This Recalled?
Product not meeting the iodine assay level requirements to support 36 month expiration dating.
Where Was This Sold?
This product was distributed to 13 states: CO, FL, GA, KY, MI, MO, NH, NC, OH, TN, TX, WA, WI
About Cypress Medical Products LLC
Cypress Medical Products LLC has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report