PlainRecalls
FDA Devices Moderate Class II Terminated

125" (318 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave¿, Remv 3 Gang 4-Way Stopcock w/Baseplate, Rotating Luer, 3 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.

Reported: August 15, 2018 Initiated: July 31, 2017 #Z-2652-2018

Product Description

125" (318 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave¿, Remv 3 Gang 4-Way Stopcock w/Baseplate, Rotating Luer, 3 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.

Reason for Recall

Some devices were labeled as Does not contain DEHP even though the product may contain small amounts of DEHP.

Details

Recalling Firm
ICU Medical, Inc.
Units Affected
160,016 units total
Distribution
Worldwide Distribution: US (nationwide) distribution to AL, AR, CA, CT, DE, FL, IA, IL, IN, KS, MA, MD, ME, MI, MO, NC, NJ, NY, OH, OR, PA, RI, TN, TX, UT, VA, WA, WV; and countries of:: Canada, Cyprus, Japan, Kuwait, MALAYSIA ,and South Africa.
Location
San Clemente, CA

Frequently Asked Questions

What product was recalled?
125" (318 cm) Y-Type Blood Set w/170 Micron Filter, Hand Pump, 3 Clave¿, Remv 3 Gang 4-Way Stopcock w/Baseplate, Rotating Luer, 3 Ext, Sterile The blood tubing accessory with CLAVE Connector is a single use, sterile, non-pyrogenic device intended for use as an adjunct to blood tubing sets or venipuncture devices for needle-free withdrawal of blood.. Recalled by ICU Medical, Inc.. Units affected: 160,016 units total.
Why was this product recalled?
Some devices were labeled as Does not contain DEHP even though the product may contain small amounts of DEHP.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 15, 2018. Severity: Moderate. Recall number: Z-2652-2018.