241-McKesson Premium Skin Staple Remover Kit — Class II medical device recall Z-0932-2018
Terminated recall by Cypress Medical Products LLC, reported 2018-03-14, distributed in CO, FL, GA, KY, MI, MO, NC, NH…. Product not meeting the iodine assay level requirements to support 36 month expiration dating.
| Recall number | Z-0932-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cypress Medical Products LLC, Richmond, VA, United States |
| Recall initiated | 2017-11-17 |
| Classified | 2018-03-08 |
| Reported by FDA | 2018-03-14 |
| Terminated | 2020-04-08 |
| Distributed | CO, FL, GA, KY, MI, MO, NC, NH, OH, TN, TX, WA, WI |
| Quantity | 12,206 cases |
| Reason classes | potency |
| Model numbers | 100123, 100124, 241, 82-15 |
Product
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.
Reason for recall
Product not meeting the iodine assay level requirements to support 36 month expiration dating.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0932-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.