# FDA recall Z-0932-2018

> **Cypress Medical Products LLC** · Class II · device recall initiated 2017-11-17.

## 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.

## Distribution

US Distribution to states of: CO, FL, GA, KY, MI, MO, NC, NH, OH, TN, TX, WA, AND WI.

## Key facts

- **Recall number:** Z-0932-2018
- **Recalling firm:** Cypress Medical Products LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-11-17
- **Report date:** 2018-03-14
- **Termination date:** 2020-04-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Richmond, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0932-2018

## Citation

> AI Analytics. FDA recall Z-0932-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0932-2018. Source: US FDA. Licensed CC0.

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