United StatesMerit Medical inflation devices—primarily basixCOMPAK 30 atm/bar 20 mL (REF numbers include ENDO-AN2030/B, IN4130/CNK and many other REF/UDI/lot numbers) and related Allwell inflation/angioplasty packs and Merit custom kits—are affected and can be identified by the listed reference, UDI and lot numbers. They were recalled because the inflation device handle may detach from the syringe during a procedure.
What's being recalled
Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Reference Numbers: ENDO-AN2030/B IN4130/CNK IN4130/H IN4130/JPH IN4130/K IN4130/KRK IN4130/L IN4130/T IN4230/JPH IN4230/K IN4330/CNK IN4330/K IN4352/K IN4430/K IN4530/CNK IN4530/K IN4530/T IN4802/K IN4802/T IN4852/K IN4901/A IN4902/A IN4903/A IN4904/A IN4905/A IN4906/A IN4907/A IN4908 IN4909 IN4910 IN4911/A IN4912 IN4913/A IN4914/A IN4915 IN4916/A IN4917/A IN4918/A IN4919/A
Allwell Inflation Device, for angiographic use REF: IS-30-A
Merit Medical , Custom Waste Management Kit Vascular Tray REF: K10T-05261
Merit Medical , Custom Inflation Kit REF: K05-00761F K05-01717B K05-02080D K05-02090C K05-02221 K05-02338 K05-02470 K05-02954 K05-03094A K05T-00380C K05T-01674B K05T-01863 K05T-01915 K05T-01920F K05T-01955 K05T-02138 K05T-02138A K05T-02272G K05T-02272H K05T-02533 K05T-03153 K05T-03201
Merit Medical , Custom Manifold Kit REF: K09-13203A
Merit Medical , Custom Procedure Kit Reference Numbers: K12T-04270A K12T-07956 K12T-10922B
Allwell Angioplasty Pack REF: IS-30-B1/B
Recalling firm: Merit Medical Systems, Inc., South Jordan, UT, United States.
How to identify it
Reference Number/UDI Number/Lot Number(s) ENDO-AN2030/B 00884450645161 I2559664 00884450645161 I2617758 00884450645161 I2622046 00884450645161 I2657805 00884450645161 I2937082 00884450645161 I3056430 00884450645161 I3085664 00884450645161 I3118225 00884450645161 I3251180 00884450645161 I3282751 IN4130/CNK 00884450636695 I2559550 00884450636695 I2559551 00884450636695 I2563338 00884450636695 I2563339 00884450636695 I2563340 00884450636695 I2564655 00884450636695 I2564665 00884450636695 I2567481 00884450636695 I2567482 00884450636695 I2567483 00884450636695 I2578099 00884450636695 I2578100 00884450636695 I2584021 00884450636695 I2584024 00884450636695 I2584025 00884450636695 I2584026 00884450636695 I2607299 00884450636695 I2607301 00884450636695 I2607302 00884450636695 I2617759 00884450636695 I2617760 00884450636695 I2628998 00884450636695 I2629000 00884450636695 I2629001 00884450636695 I2629002 00884450636695 I2630702 00884450636695 I2648658 00884450636695 I2648659 00884450636695 I2648660 00884450636695 I2648661 00884450636695 I2657828 00884450636695 I2657833 00884450636695 I2657884 00884450636695 I2657889 00884450636695 I2663025 00884450636695 I2663026 00884450636695 I2663027 00884450636695 I2669899 00884450636695 I2669900 00884450636695 I2674531 00884450636695 I2674532 00884450636695 I2682701 00884450636695 I2682702 00884450636695 I2684463 00884450636695 I2684522 00884450636695 I2684523 00884450636695 I2699591 00884450636695 I2699592 00884450636695 I2703002 00884450636695 I2703003 00884450636695 I2703004 00884450636695 I2703006 00884450636695 I2703081 00884450636695 I2703082 00884450636695 I2703083 00884450636695 I2707735 00884450636695 I2707736 00884450636695 I2715012 00884450636695 I2715013 00884450636695 I2719928 00884450636695 I2719929 00884450636695 I2719930 00884450636695 I2719931 00884450636695 I2719933 00884450636695 I2752077 00884450636695 I2752078 00884450636695 I2755218 00884450636695 I2755219 00884450636695 I2755496 00884450636695 I2760565…
The hazard
Inflation device handle may detach from the syringe during procedure.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VI, VT, WA, WI, WV, WY, St. Thomas , Puerto Rico and the countries of Albania, Algeria, Angola, Argentina, Australia, Austria, Bahrain, Barbados, Belgium, Brazil, Bulgaria, Cambodia, Canada, Cayman Islands, Chile, China, Colombia, Cote d'Ivoire, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, El Salvador, Finland, France, Germany, Greece, Guatemala, Honduras, Hong Kong, Iceland, India, Indonesia, Ireland, Israel, Italy, Jamaica, Japan, Kazakhstan, Korea, Republic of Kuwait, Kyrgyzstan, Latvia, Lebanon, Libya, Luxembourg, Madagascar, Mexico, Monaco, Nepal, Netherlands, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Panama, Paraguay, Peru, Poland, Portugal, Qatar, Romania, Russian Federation, Rwanda, San Marino, Saudi Arabia, Serbia, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan, Trinidad and Tobago, Uganda, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Venezuela, Bolivarian, Republic of Viet Nam.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)