The FDA announced on June 27, 2022, that ICU Medical, Inc. is recalling ChemoLock Bag Spike and related products due to a potential for unintended disconnection of ports. This defect may cause delays in therapy and exposure to caustic substances. The recall affects approximately 454,635 units distributed worldwide.
How to tell if you have it
- Brand: ICU Medical
- Product: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY SPIKE/CL-12; APPX 1.5ml,ChemoLock BAG SPIKE WITH ADDITIVE PORT/CL-13; ChemoLock Port/CL2100; ChemoLock Port, 5 Units/CL2100-5; ChemoLock Port/CL2100T; Clave Bag Spike w ChemoLock Port/CL2150; 30" (76 cm) Appx 3.3 ml, 20 Drop Admin Set w Integrated ChemoLock Drip Chamber, Spiros w/Red Cap, Hanger/CL3011; 9 IN(23cm)APPX 2.7ml,EXT SET,ChemoLock PORT,2 CLAMPS,2 GRADUATED CONN/CL3364; Syringe Transfer Set w Clave, ChemoLock Port/CL-34; 30" (76 cm) Appx 3.6 ml, 20 Drop Admin Set w Integrated ChemoLock Port Drip Chamber, ChemoLock w Red Cap, Bag Hanger/CL3511; 30" (76 cm) Appx 3.6 ml, 20 Drop Admin Set w Integrated ChemoLock Port Drip Chamber, ChemoLock w Red Cap, Bag Hanger/CL3511T; 30" (76cm) Appx 6.3 ml, 20 Drop Admin Set w Integrated ChemoLock Port Drip Chamber, 0.2 Micron Filter, ChemoLock w Red Cap, Hanger/CL3528; 7" (18 cm) Appx .93 ml, Ext Set w/ChemoLock, Y-Connector, Rotating Luer/CL3535T; Oncology Kit w/5" (13 cm) Add-On Set w ChemoLock Additive Port, Vented Cap, ChemoLock, Spinning Spiros w Red Cap/CL3538; Graduated Connector w ChemoLock Port/CL3900; ONCOLOGY KIT, EXT,ChemoLock PORT, GRAD CONN,TRANSFER,ChemoLock,VIAL SPIKE,ChemoLock PORT/CL3927; Oncology Kit w 5" (13 cm) Add-On Set w ChemoLock w Red Cap, Vented Cap, ChemoLock Port w Bag Spike, Spiros w Red Cap/CL3946; Oncology Kit w 17" (43 cm) Bifuse Ext Set w/ChemoLock w Red Cap, ChemoLock Port, ChemoLock Vented Vial Spike, 13mm ChemoLock/CL3947; Oncology Kit w ChemoLock Port Closed Vial Spike, ChemoLock, ChemoLock Port Bag Spike/CL3952; APPX 0.5ml, ChemoLock BAG SPIKE WITH ADDITIVE PORT,ChemoLock Port/CL3955; CL3960; CL3963; CL4114; CL4130; CL4131; CL4136; CL4143; CL4146-5; CL4153; CL4159; CL4179; CL-62; CL-70; CL-70-10; CL-70-10T; CL-70S; CL-70S-5; CL-70T; CL-72; CL-72T; CL-76; CL-80; CL-80S; CL-80S-10; CL-80S-10T; CL-80S-5; CL-80SL; CL-82; CLH-12
- Units affected: 454,635
- Distribution: US Nationwide and countries including Saudi Arabia, Australia, United Arab Emirates, Spain, Slovenia, Japan, Canada
The hazard
According to the FDA, ports have a potential for unintended disconnection or inability to connect to or fully engage with injectors due to a variation in the spring inside the Port. This defect may cause delay of therapy and exposure to caustic substances.
Context
GovInfoNow's records show ICU Medical, Inc. has 60 other recalls on record since June 15, 2017. Other recent recalls include the ICU Medical CADD Yellow Medication Cassette Reservoir Recall (August 20, 2026), the ICU Medical Hotline Fluid Warming Set Recall (June 24, 2026), and a recall regarding pump decrement errors (June 10, 2026). Other recent recalls of similar products include the Medline Medical Procedure Kits Recall (May 4, 2026) and Mozarc Medical Acute High Pressure Catheter Tray Extensions Recall (October 17, 2025).