PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: March 14, 2018 Initiated: November 17, 2017 #Z-0932-2018

Product Description

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.

Details

Units Affected
12,206 cases
Distribution
US Distribution to states of: CO, FL, GA, KY, MI, MO, NC, NH, OH, TN, TX, WA, AND WI.
Location
Richmond, VA

Frequently Asked Questions

What product was recalled?
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.. Recalled by Cypress Medical Products LLC. Units affected: 12,206 cases.
Why was this product recalled?
Product not meeting the iodine assay level requirements to support 36 month expiration dating.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 14, 2018. Severity: Moderate. Recall number: Z-0932-2018.