Recall Z-0629-2024

Merit Medical Systems, Inc. · initiated November 6, 2023

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Fountain, REF: IS4-135-30 and IS4-90-10, CE2797, STERILEEO, Rx ONLY

Codes / lots: REF: IS4-135-30 Lot # H2765720 UDI: 00884450000885 REF: IS4-90-10 Lot # H2765603 UDI: 00884450006504

Reason for recall

The sterility of microcatheter and infusion system devices cannot be guaranteed.

FDA-determined cause: Package design/selection

Action taken

On November 6, 2023, Merit Medical issued a Urgent Medical Device Recall Notice to affected consignees via Email or UPS. Merit Medical asked consignees to take the following actions: 1. Immediately determine if any of the devices identified in the attached Customer Response Form (CRF) are within your facility, quarantine them, and discontinue use and distribution. 2. Ensure that applicable personnel within your organization are made aware of this field action. 3. If the product has been further distributed to other facilities, institutions, or manufacturers, please ensure this notice is immediately shared with them and note the quantity distributed on the CRF. Additional distribution details may be required by health authorities. 4. Please fill out, scan and email the completed Customer Response Form to Customer Service at response@merit.com within seven (7) days. All affected product shipped to you must be accounted for on the CRF. 5. Please immediately return all affected lots in your possession to Merit, per the instructions in the attached CRF.

Details

Recall number
Z-0629-2024
Initiated
November 6, 2023
Posted by FDA
January 2, 2024
Product code
QEY – Mechanical Thrombolysis Catheter
Quantity
3 units
Distribution
Worldwide - US Nationwide distribution in the states of AL, AZ, CA, CO, CT, FL, IA, IL, IN, KS, MA, MD, MN, MO, NH, NJ, NSW, NV, NY, UT, WI and the countries of Argentina, Australia, Belgium, China, France, Germany, Guam, Hong Kong, Italy, Mexico, Netherlands, Switzerland.
Recalling firm
Merit Medical Systems, Inc., South Jordan, UT

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-0627-2024 Class IIMerit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B…The sterility of microcatheter and infusion system devices cannot be guaranteed. 11/06/2023Open, Classified
Z-0628-2024 Class IIMerit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A…The sterility of microcatheter and infusion system devices cannot be guaranteed. 11/06/2023Open, Classified