FDA recall Z-0526-2020

Product

Various Custom Products, Item Nos. CP102940 CP102941 CP102942 CP102943 CP102944 CP102945 CP102946 CP102947 CP102948 CP112662 CP112663 CP112664 CP112674 CP112675 CP113771 CP113777 CP113778 CP113782 CP113783 CP114083 CP114090 CP114112 CP114118 CP114148 CP114213 CP114388 CP114436 CP114463 CP114472 CP114478 CP114495 CP114532 CP114561 CP114563 CP114605 CP114695 CP114756 CP114782 CP114783 CP114933 CP114987 CP115008 CP115048 CP115049 CP115050 CP115166 CP115209 CP115212 CP115312 CP115313 CP115314 CP115318 CP115319 CP115320 CP115322 CP115357 CP115358 CP115359 CP115360 CP115362 CP115363 CP115371 CP161304 CP161305 CP161306 CP161307 CP161522 CP161560 CP161735 CP161741 CP161751 CP161752 CP161753 CP161768 CP161793 CP161795 CP161831 CP161867 CP162006 CP162007 CP162008 CP162013 CP162017 CP162042 CP162043 CP162055 CP162084 CP162085 CP162086 CP162121 CP162149 CP162150 PM0000711 PM103016 PM103022 PM103060 PM15

Reason for recall

Elevated levels of bacterial endotoxin and residual debris remain on the devices due to cleaning issue.

Distribution

US Nationwide distribution and countries of Argentina, Australia, Brazil, Canada, Chile, Colombia, Costa Rica, Ecuador, El Salvador, Italy, Netherlands, India, Japan, Korea, Malaysia, Mexico, New Zealand, Panama, Singapore, Taiwan, Thailand, Trinidad and Tobago, and Venezuela.

Key facts

Status

Terminated

Initiation date

2019-08-21

Report date

2019-12-04

Termination date

2021-07-21

Voluntary/Mandated

Voluntary: Firm initiated

Location

Warsaw, IN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0526-2020