Cypress Medical Products recalls 241-McKesson Premium Skin Staple Remover Kit and related items due to iodine assay levels not meeting 36-month expiration requirements. Consumers should contact the manufacturer for details.
“Cypress Medical Products Skin Staple Remover Kit Recall: Iodine Assay Issue.” GovInfoNow, updated September 1, 2026. https://govinfonow.com/recall/72526-cypress-medical-products-skin-staple-remover-kit-recall-iodine-assay. Based on FDA recall #Z-0932-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0932-2018%22&limit=1).
The FDA announced on 2017-11-17 that Cypress Medical Products LLC voluntarily recalled specific McKesson and Cypress skin staple remover kits due to failing iodine assay level requirements for their expiration dating. The agency issued recall number Z-0932-2018 for the Class II device.
Product: 82-15 Cypress Medical Products Skin Staple Remover Kit
McKesson Items: 241, 100123, 100124
Cypress Item: 82-15
The hazard
The recalled products do not meet the iodine assay level requirements necessary to support a 36-month expiration dating. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Cypress Medical Products LLC has had 7 other recalls on record since 2018-07-02. Recent brand recalls include the 2024-08-20 BinaxNOW Strep A Test Kit Recall for license purchase errors and the 2024-08-06 recall of 60mL syringes lacking FDA clearance. Other recent recalls of similar products include Cook Medical Blue Rhino G2 Tracheostomy Tray Recall (2026-03-05) and Cook Medical Spectrum Central Venous Tray Recall (2026-03-05).
How to tell if you have this one
Check for the product names: 241-McKesson Premium Skin Staple Remover Kit (Item #100123), McKesson I.V. Start Kit (Item #100124), or Cypress Skin Staple Remover Kit (Item #82-15). These were sold through McKesson.
Brand
Cypress Medical Products
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Contact Manufacturer
Reach out to Cypress Medical Products for specific instructions on handling the recalled items.
Where it went and when
Where it was distributed
Distributed in 13 states.
Listed by the agency
Not listed
FDA distribution: “US Distribution to states of: CO, FL, GA, KY, MI, MO, NC, NH, OH, TN, TX, WA, AND WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Florida, Georgia, Kentucky, Michigan, Missouri, New Hampshire, North Carolina, Ohio, Tennessee, Texas, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 2.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0932-2018 (November 17, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0932-2018 to see it in context.
Plain-language summary written by qwen3:4b on September 1, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.