PlainRecalls
FDA Devices Moderate Class II Terminated

Stamey Needle

Reported: June 21, 2017 Initiated: April 25, 2017 #Z-2536-2017

Product Description

Stamey Needle

Reason for Recall

reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products

Details

Recalling Firm
Cook Inc.
Units Affected
698
Distribution
The devices have been distributed nationwide within the United States and the following countries: Australia, Belgium, Canada, Finland, Germany, Guatemala, Hong Kong, India, Ireland, Japan, South Korea, Kuwait, Malaysia, Netherlands, New Zealand, Puerto Rico, Saudi Arabia, Taiwan, and the United Kingdom.
Location
Bloomington, IN

Frequently Asked Questions

What product was recalled?
Stamey Needle. Recalled by Cook Inc.. Units affected: 698.
Why was this product recalled?
reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products
Which agency issued this recall?
This recall was issued by the FDA Devices on June 21, 2017. Severity: Moderate. Recall number: Z-2536-2017.