FDA Medical Device Recalls (openFDA)
CYPRESS MEDICAL PRODUCTS: McKesson Powder Free Vinyl Exam Gloves Catalog numbers 14-116, 14-118, 14-120, 14-136, 14-138 and 14-140
- Recall number
- Z-0741-2017
- Recalling firm
- CYPRESS MEDICAL PRODUCTS
- Product
- McKesson Powder Free Vinyl Exam Gloves Catalog numbers 14-116, 14-118, 14-120, 14-136, 14-138 and 14-140
- Status
- Terminated
- Initiated
- 2016-10-12
- Posted
- 2016-12-12
- Terminated
- 2017-03-27
- Reason
- A container of McKesson vinyl gloves that failed the FDA leak test was inadvertently distributed.
- Root cause
- Process control
- Action
- A letter, dated October 19, 2016, on Cypress Medical Products letterhead, was sent to customers. Customers were requested to stop use and quarantine the gloves.
- Quantity
- 2005.2 cases have been distributed
- Distribution
- US Distribution. This recall is limited to one distribution center in Auburn, Washington, and the customers serviced from that distribution center.
- Lot, serial or model codes
- Lot Number: CDZF06-03
- 510(k) numbers
- ["K120968"]
- PMA numbers
- not on file
- Product code
- LYZ
- Firm FEI
- 1451040
- Firm city
- Richmond
- Firm state
- VA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28