PlainRecalls
FDA Devices Moderate Class II Terminated

Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K

Reported: February 17, 2021 Initiated: January 7, 2021 #Z-1082-2021

Product Description

Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K

Reason for Recall

Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.

Details

Recalling Firm
Cardinal Health 200, LLC
Units Affected
137,346 kits
Distribution
Global Distribution. US Nationwide.
Location
Waukegan, IL

Frequently Asked Questions

What product was recalled?
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K. Recalled by Cardinal Health 200, LLC. Units affected: 137,346 kits.
Why was this product recalled?
Gowns included in the kits potentially have rips, holes, tears, incomplete and/or open seams, staining, foreign material or debris on the gowns.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 17, 2021. Severity: Moderate. Recall number: Z-1082-2021.