PlainRecalls
FDA Devices Moderate Class II Terminated

JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;

Reported: April 25, 2018 Initiated: February 23, 2017 #Z-1425-2018

Product Description

JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;

Reason for Recall

The integrity of the sterile packaging is potentially compromised.

Details

Recalling Firm
Carefusion 2200 Inc
Units Affected
14,200 units
Distribution
Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam
Location
Vernon Hills, IL

Frequently Asked Questions

What product was recalled?
JAMSHIDI (TJ) NEEDLE BM ASP MAC [a.) 13G x 3.5, b.) 8G x 4, c.) 11G x 3.5, d.) 8G x 6, e.) 11G x 6]; STERILE;. Recalled by Carefusion 2200 Inc. Units affected: 14,200 units.
Why was this product recalled?
The integrity of the sterile packaging is potentially compromised.
Which agency issued this recall?
This recall was issued by the FDA Devices on April 25, 2018. Severity: Moderate. Recall number: Z-1425-2018.